FDA NDC Directory · JSON-LD · Markdown

Progesterone

NDC 63323-261 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namePROGESTERONE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075906
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR
Active ingredientsPROGESTERONE (50 mg/mL)
Marketing started20010719
Package count1

External sources

Source: openFDA. Public-domain (CC0).