# Follistim AQ

NDC: 78206-129
Generic name: follitropin
Labeler / Manufacturer: Organon LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20230724

FDA application: BLA021211

## Active ingredients

- FOLLITROPIN: 300 [iU]/.36mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"78206-129"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=78206-129
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=48489027-e52b-4b10-ae74-4ba03839150c