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Cyproheptadine Hydrochloride

NDC 27808-099 · HUMAN PRESCRIPTION DRUG · SYRUP

Labeler / ManufacturerTris Pharma Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA205431
Dosage form / routeSYRUP · ORAL
Active ingredientsCYPROHEPTADINE HYDROCHLORIDE (2 mg/5mL)
Marketing started20211221
Package count1

External sources

Source: openFDA. Public-domain (CC0).