growth hormone
Brand names: Norditropin, Genotropin
This medicine is a growth hormone. It may help your body's defenses and relieve some symptoms.
Drug Pricing (NADAC)
Brand Price
$1715.73/unit
Generic Available
No
Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →
What it does
This medicine may help with a tendency to catch colds or the flu.
Common side effects
No common side effects listed.
Key warnings
The FDA has not evaluated these claims.
How It Works
This medicine is a recombinant human growth hormone. It works by supplementing your body's natural growth hormone.
How to Take It
Adults only should use this medicine. Spray it two times under your tongue. Do this three times each day. One bottle should last about a month.
Pregnancy & Breastfeeding
There is no information about the safety of this medicine during pregnancy or breastfeeding. Talk to your doctor before use if you are pregnant or breastfeeding.
Missed Dose
If you miss a dose, just take your next dose as scheduled. Do not double your dose.
Storage
Store this medicine as directed on the package.
Serious Warnings
The FDA has not evaluated these claims.
Common Questions
How long will it take to see results?
Can children use this medicine?
How many times a day should I use the spray?
How long will one bottle last?
What if I don't see any improvement?
Is this medicine FDA approved?
What should I do if I experience side effects?
Can I take this with other medications?
What do I do if I miss a dose?
How should I store this medicine?
What drug class is growth hormone?
Is growth hormone safe during pregnancy?
Related Medications in Recombinant Human Growth Hormone
Other drugs grouped near growth hormone — same-class peers and common alternatives.
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clomiphene
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What the FDA Data Shows for growth hormone
The FDA label for growth hormone (sold under brand names such as Norditropin, Genotropin) classifies it as a prescription-only medication in the Recombinant Human Growth Hormone class. This medicine may help with a tendency to catch colds or the flu. Labeling covers dosing, contraindications, and monitoring requirements derived from clinical trials.
Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. Voluntary reports accumulate over the lifetime of a drug and reflect wide-ranging clinical use. Interaction data is drawn directly from FDA-approved prescribing information. NADAC pricing from CMS.
Report counts do not establish causation — a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.
Data Sources
Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).
FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.
Last updated: January 31, 2025
Read our methodology — how this data is sourced, computed, and verified.
All federal data sources used on this page
- FDA Orange Book — approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed — NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) — post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm — standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files — federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database — current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages