THIS SITE IS INTENDED FOR U.S. HEALTHCARE PROFESSIONALS ONLY

Cost should not stand in the way of your child’s growth

ZOMACTON offers savings programs that can help make every inch more affordable*
Even if you have prescription drug coverage, you may be surprised by the low out-of-pocket costs of ZOMACTON*

ZOMACTON is available at the specialty pharmacies listed below

Share these pharmacies with your doctor when discussing ZOMACTON as a treatment option.

University Compounding Pharmacy

Ocean Breeze Healthcare

Transition Pharmacy Services

Kroger Specialty Pharmacy

Don’t have
health insurance?

Calculate your estimated monthly cost for ZOMACTON

See an estimation of what you may pay out-of-pocket for prescription ZOMACTON.

Enter milligrams of somatropin prescribed by your healthcare provider per month and select “Calculate”

Enter milligrams of somatropin prescribed by your healthcare provider per month and select “Calculate”

mg/month
=
Estimated monthly cash price for ZOMACTON
$20
per month
Additional discounts may apply
See terms and conditions
“Is it too much to ask for a growth hormone that not only works,
but offers savings to help fit
within my family’s budget?”

ZOMACTON gives you enhanced savings support every inch of the way

Provides a range of financial assistance programs for eligible patients

Save up to $500 per month for eligible patients with prescription drug coverage*

Significant savings from the first prescription for cash-paying patients

Some patients may pay as little as $0 per prescription1

Helpful resources

ZOMACTON 5mg
Pocket Guide
ZOMACTON 10mg
Pocket Guide

*Individual out-of-pocket costs for eligible patients may vary based upon a variety of factors, including your specific insurance plan requirements.

The ZOMACTON Cost Calculator is intended for informational purposes only.

References: 1. Data on file, Ferring Pharmaceuticals.

ZOMACTON (somatropin) for Injection

Indications

ZOMACTON is a recombinant human growth hormone (GH) indicated for the treatment of pediatric patients with:

  • growth failure due to inadequate secretion of endogenous GH
  • short stature associated with Turner syndrome
  • idiopathic short stature (ISS)
  • short stature or growth failure in short stature homeobox-containing gene (SHOX) deficiency
  • short stature born small for gestational age (SGA) with no catch-up growth by 2 to 4 years

ZOMACTON is also indicated for the replacement of endogenous GH in adults with GH deficiency.

Contraindications

ZOMACTON is contraindicated in patients with:

  • acute critical illness
  • pediatric patients with Prader-Willi syndrome who are severely obese, have a history of upper airway obstruction or sleep apnea, or have severe respiratory impairment due to the risk of death
  • active malignancy
  • hypersensitivity to ZOMACTON, its excipients, or diluents. Systemic hypersensitivity reactions, including anaphylaxis and angioedema, have been reported with postmarketing use of somatropins
  • active proliferative or severe non-proliferative diabetic retinopathy
  • pediatric patients with closed epiphyses

Warnings and Precautions

Increased Risk of Neoplasm: Second neoplasms have occurred in childhood cancer survivors. Monitor patients with preexisting tumors for progression or recurrence.

Glucose Intolerance and Diabetes Mellitus: ZOMACTON may decrease insulin sensitivity, particularly at higher doses. Monitor glucose levels periodically, especially in patients with existing diabetes mellitus or at risk for development.

Intracranial Hypertension (IH): Has been reported usually within 8 weeks of initiation. Perform fundoscopic examinations prior to initiation and periodically thereafter. If papilledema occurs, stop treatment.

Hypersensitivity: Serious hypersensitivity reactions may occur, including anaphylaxis and angioedema; seek prompt medical attention.

Fluid Retention: May occur in adults and may be dose dependent.

Hypoadrenalism: Monitor patients for reduced serum cortisol levels or need for glucocorticoid dose increases in those with known hypoadrenalism.

Hypothyroidism: Monitor thyroid function periodically as hypothyroidism may occur or worsen after initiation of somatropin.

Slipped Capital Femoral Epiphysis in Pediatric Patients: May occur; evaluate patients with onset of a limp or hip/knee pain for slipped capital femoral epiphysis and osteonecrosis and manage accordingly.

Progression of Preexisting Scoliosis in Pediatric Patients: Monitor patients with scoliosis for progression.

Pancreatitis: Has been reported; consider pancreatitis in patients with abdominal pain, especially pediatric patients.

Risk of Serious Adverse Reactions in Infants due to Benzyl Alcohol Preservative: Serious and fatal adverse reactions can occur in neonates and infants treated with benzyl alcohol-preserved drugs, including the diluent for ZOMACTON 5 mg. If administering ZOMACTON 5 mg to infants, reconstitute with 0.9% sodium chloride injection.

Adverse Reactions

Common adverse reactions reported include: upper respiratory infection, fever, pharyngitis, headache, otitis media, edema, arthralgia, paresthesia, myalgia, carpal tunnel syndrome, peripheral edema, flu syndrome, hypothyroidism, hyperglycemia, and impaired glucose tolerance.

Drug Interactions

Glucocorticoids: Patients treated with glucocorticoids may require an increased dose.

Pharmacologic Glucocorticoid Therapy and Supraphysysiologic Glucocorticoid Treatment: Adjust dosing in pediatric patients to avoid hypoadrenalism or an inhibitory effect on growth.

Cytochrome P450-Metabolized Drugs: Monitor carefully if used with ZOMACTON as clearance may be altered.

Oral Estrogen: Larger doses of ZOMACTON may be required.

Insulin or Other Hypoglycemic Agents: Dose adjustment may be required.

Use In Specific Populations

Pregnancy and Lactation: If ZOMACTON 5 mg is needed, reconstitute with 0.9% sodium chloride injection or use the ZOMACTON 10 mg benzyl alcohol-free formulation.

Please see Full Prescribing Information for ZOMACTON.

ZOMACTON (somatropin) for Injection

Important Safety Information

Contraindications

ZOMACTON is contraindicated in patients with:

  • acute critical illness
  • pediatric patients with Prader-Willi syndrome who are severely obese, have a history of upper airway obstruction or sleep apnea, or have severe respiratory impairment due to the risk of death
  • active malignancy
  • hypersensitivity to ZOMACTON, its excipients, or diluents. Systemic hypersensitivity reactions, including anaphylaxis and angioedema, have been reported with postmarketing use of somatropins
  • active proliferative or severe non-proliferative diabetic retinopathy
  • pediatric patients with closed epiphyses

Warnings and Precautions

Increased Risk of Neoplasm: Second neoplasms have occurred in childhood cancer survivors. Monitor patients with preexisting tumors for progression or recurrence.

Glucose Intolerance and Diabetes Mellitus: ZOMACTON may decrease insulin sensitivity, particularly at higher doses. Monitor glucose levels periodically, especially in patients with existing diabetes mellitus or at risk for development.

Intracranial Hypertension (IH): Has been reported usually within 8 weeks of initiation. Perform fundoscopic examinations prior to initiation and periodically thereafter. If papilledema occurs, stop treatment.

Hypersensitivity: Serious hypersensitivity reactions may occur, including anaphylaxis and angioedema; seek prompt medical attention.

Fluid Retention: May occur in adults and may be dose dependent.

Hypoadrenalism: Monitor patients for reduced serum cortisol levels or need for glucocorticoid dose increases in those with known hypoadrenalism.

Hypothyroidism: Monitor thyroid function periodically as hypothyroidism may occur or worsen after initiation of somatropin.

Slipped Capital Femoral Epiphysis in Pediatric Patients: May occur; evaluate patients with onset of a limp or hip/knee pain for slipped capital femoral epiphysis and osteonecrosis and manage accordingly.

Progression of Preexisting Scoliosis in Pediatric Patients: Monitor patients with scoliosis for progression.

Pancreatitis: Has been reported; consider pancreatitis in patients with abdominal pain, especially pediatric patients.

Risk of Serious Adverse Reactions in Infants due to Benzyl Alcohol Preservative: Serious and fatal adverse reactions can occur in neonates and infants treated with benzyl alcohol-preserved drugs, including the diluent for ZOMACTON 5 mg. If administering ZOMACTON 5 mg to infants, reconstitute with 0.9% sodium chloride injection.

Adverse Reactions

Common adverse reactions reported include: upper respiratory infection, fever, pharyngitis, headache, otitis media, edema, arthralgia, paresthesia, myalgia, carpal tunnel syndrome, peripheral edema, flu syndrome, hypothyroidism, hyperglycemia, and impaired glucose tolerance.

Drug Interactions

Glucocorticoids: Patients treated with glucocorticoids may require an increased dose.

Pharmacologic Glucocorticoid Therapy and Supraphysysiologic Glucocorticoid Treatment: Adjust dosing in pediatric patients to avoid hypoadrenalism or an inhibitory effect on growth.

Cytochrome P450-Metabolized Drugs: Monitor carefully if used with ZOMACTON as clearance may be altered.

Oral Estrogen: Larger doses of ZOMACTON may be required.

Insulin or Other Hypoglycemic Agents: Dose adjustment may be required.

Use In Specific Populations

Pregnancy and Lactation: If ZOMACTON 5 mg is needed, reconstitute with 0.9% sodium chloride injection or use the ZOMACTON 10 mg benzyl alcohol-free formulation.

Please see Full Prescribing Information for ZOMACTON.

Indications

ZOMACTON is a recombinant human growth hormone (GH) indicated for the treatment of pediatric patients with:

  • growth failure due to inadequate secretion of endogenous GH
  • short stature associated with Turner syndrome
  • idiopathic short stature (ISS)
  • short stature or growth failure in short stature homeobox-containing gene (SHOX) deficiency
  • short stature born small for gestational age (SGA) with no catch-up growth by 2 to 4 years

ZOMACTON is also indicated for the replacement of endogenous GH in adults with GH deficiency.

ZOMACTON (somatropin) for Injection

Indications

ZOMACTON is a recombinant human growth hormone (GH) indicated for the treatment of pediatric patients with:

  • growth failure due to inadequate secretion of endogenous GH
  • short stature associated with Turner syndrome
  • idiopathic short stature (ISS)
  • short stature or growth failure in short stature homeobox-containing gene (SHOX) deficiency
  • short stature born small for gestational age (SGA) with no catch-up growth by 2 to 4 years

ZOMACTON is also indicated for the replacement of endogenous GH in adults with GH deficiency.

Contraindications

ZOMACTON is contraindicated in patients with:

  • acute critical illness
  • pediatric patients with Prader-Willi syndrome who are severely obese, have a history of upper airway obstruction or sleep apnea, or have severe respiratory impairment due to the risk of death
  • active malignancy
  • hypersensitivity to ZOMACTON, its excipients, or diluents. Systemic hypersensitivity reactions, including anaphylaxis and angioedema, have been reported with postmarketing use of somatropins
  • active proliferative or severe non-proliferative diabetic retinopathy
  • pediatric patients with closed epiphyses

Warnings and Precautions

Increased Risk of Neoplasm: Second neoplasms have occurred in childhood cancer survivors. Monitor patients with preexisting tumors for progression or recurrence.

Glucose Intolerance and Diabetes Mellitus: ZOMACTON may decrease insulin sensitivity, particularly at higher doses. Monitor glucose levels periodically, especially in patients with existing diabetes mellitus or at risk for development.

Intracranial Hypertension (IH): Has been reported usually within 8 weeks of initiation. Perform fundoscopic examinations prior to initiation and periodically thereafter. If papilledema occurs, stop treatment.

Hypersensitivity: Serious hypersensitivity reactions may occur, including anaphylaxis and angioedema; seek prompt medical attention.

Fluid Retention: May occur in adults and may be dose dependent.

Hypoadrenalism: Monitor patients for reduced serum cortisol levels or need for glucocorticoid dose increases in those with known hypoadrenalism.

Hypothyroidism: Monitor thyroid function periodically as hypothyroidism may occur or worsen after initiation of somatropin.

Slipped Capital Femoral Epiphysis in Pediatric Patients: May occur; evaluate patients with onset of a limp or hip/knee pain for slipped capital femoral epiphysis and osteonecrosis and manage accordingly.

Progression of Preexisting Scoliosis in Pediatric Patients: Monitor patients with scoliosis for progression.

Pancreatitis: Has been reported; consider pancreatitis in patients with abdominal pain, especially pediatric patients.

Risk of Serious Adverse Reactions in Infants due to Benzyl Alcohol Preservative: Serious and fatal adverse reactions can occur in neonates and infants treated with benzyl alcohol-preserved drugs, including the diluent for ZOMACTON 5 mg. If administering ZOMACTON 5 mg to infants, reconstitute with 0.9% sodium chloride injection.

Adverse Reactions

Common adverse reactions reported include: upper respiratory infection, fever, pharyngitis, headache, otitis media, edema, arthralgia, paresthesia, myalgia, carpal tunnel syndrome, peripheral edema, flu syndrome, hypothyroidism, hyperglycemia, and impaired glucose tolerance.

Drug Interactions

Glucocorticoids: Patients treated with glucocorticoids may require an increased dose.

Pharmacologic Glucocorticoid Therapy and Supraphysysiologic Glucocorticoid Treatment: Adjust dosing in pediatric patients to avoid hypoadrenalism or an inhibitory effect on growth.

Cytochrome P450-Metabolized Drugs: Monitor carefully if used with ZOMACTON as clearance may be altered.

Oral Estrogen: Larger doses of ZOMACTON may be required.

Insulin or Other Hypoglycemic Agents: Dose adjustment may be required.

Use In Specific Populations

Pregnancy and Lactation: If ZOMACTON 5 mg is needed, reconstitute with 0.9% sodium chloride injection or use the ZOMACTON 10 mg benzyl alcohol-free formulation.

Please see Full Prescribing Information for ZOMACTON.

ZOMACTON (somatropin) for Injection

Important Safety Information

Contraindications

ZOMACTON is contraindicated in patients with:

  • acute critical illness
  • pediatric patients with Prader-Willi syndrome who are severely obese, have a history of upper airway obstruction or sleep apnea, or have severe respiratory impairment due to the risk of death
  • active malignancy
  • hypersensitivity to ZOMACTON, its excipients, or diluents. Systemic hypersensitivity reactions, including anaphylaxis and angioedema, have been reported with postmarketing use of somatropins
  • active proliferative or severe non-proliferative diabetic retinopathy
  • pediatric patients with closed epiphyses

Warnings and Precautions

Increased Risk of Neoplasm: Second neoplasms have occurred in childhood cancer survivors. Monitor patients with preexisting tumors for progression or recurrence.

Glucose Intolerance and Diabetes Mellitus: ZOMACTON may decrease insulin sensitivity, particularly at higher doses. Monitor glucose levels periodically, especially in patients with existing diabetes mellitus or at risk for development.

Intracranial Hypertension (IH): Has been reported usually within 8 weeks of initiation. Perform fundoscopic examinations prior to initiation and periodically thereafter. If papilledema occurs, stop treatment.

Hypersensitivity: Serious hypersensitivity reactions may occur, including anaphylaxis and angioedema; seek prompt medical attention.

Fluid Retention: May occur in adults and may be dose dependent.

Hypoadrenalism: Monitor patients for reduced serum cortisol levels or need for glucocorticoid dose increases in those with known hypoadrenalism.

Hypothyroidism: Monitor thyroid function periodically as hypothyroidism may occur or worsen after initiation of somatropin.

Slipped Capital Femoral Epiphysis in Pediatric Patients: May occur; evaluate patients with onset of a limp or hip/knee pain for slipped capital femoral epiphysis and osteonecrosis and manage accordingly.

Progression of Preexisting Scoliosis in Pediatric Patients: Monitor patients with scoliosis for progression.

Pancreatitis: Has been reported; consider pancreatitis in patients with abdominal pain, especially pediatric patients.

Risk of Serious Adverse Reactions in Infants due to Benzyl Alcohol Preservative: Serious and fatal adverse reactions can occur in neonates and infants treated with benzyl alcohol-preserved drugs, including the diluent for ZOMACTON 5 mg. If administering ZOMACTON 5 mg to infants, reconstitute with 0.9% sodium chloride injection.

Adverse Reactions

Common adverse reactions reported include: upper respiratory infection, fever, pharyngitis, headache, otitis media, edema, arthralgia, paresthesia, myalgia, carpal tunnel syndrome, peripheral edema, flu syndrome, hypothyroidism, hyperglycemia, and impaired glucose tolerance.

Drug Interactions

Glucocorticoids: Patients treated with glucocorticoids may require an increased dose.

Pharmacologic Glucocorticoid Therapy and Supraphysysiologic Glucocorticoid Treatment: Adjust dosing in pediatric patients to avoid hypoadrenalism or an inhibitory effect on growth.

Cytochrome P450-Metabolized Drugs: Monitor carefully if used with ZOMACTON as clearance may be altered.

Oral Estrogen: Larger doses of ZOMACTON may be required.

Insulin or Other Hypoglycemic Agents: Dose adjustment may be required.

Use In Specific Populations

Pregnancy and Lactation: If ZOMACTON 5 mg is needed, reconstitute with 0.9% sodium chloride injection or use the ZOMACTON 10 mg benzyl alcohol-free formulation.

Please see Full Prescribing Information for ZOMACTON.

Indications

ZOMACTON is a recombinant human growth hormone (GH) indicated for the treatment of pediatric patients with:

  • growth failure due to inadequate secretion of endogenous GH
  • short stature associated with Turner syndrome
  • idiopathic short stature (ISS)
  • short stature or growth failure in short stature homeobox-containing gene (SHOX) deficiency
  • short stature born small for gestational age (SGA) with no catch-up growth by 2 to 4 years

ZOMACTON is also indicated for the replacement of endogenous GH in adults with GH deficiency.