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Progesterone

NDC 76420-073 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211285
Dosage form / routeCAPSULE · ORAL
Active ingredientsPROGESTERONE (200 mg/1)
Marketing started20181026
Package count3

External sources

Source: openFDA. Public-domain (CC0).