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Clomiphene Citrate

NDC 31722-541 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCamber Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA220673
Dosage form / routeTABLET · ORAL
Active ingredientsCLOMIPHENE CITRATE (50 mg/1)
Marketing started20260831
Package count2

External sources

Source: openFDA. Public-domain (CC0).