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CLOMIPRAMINE HYDROCHLORIDE

NDC 51672-4012 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameClomipramine Hydrochloride
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074694
Dosage form / routeCAPSULE · ORAL
Active ingredientsCLOMIPRAMINE HYDROCHLORIDE (50 mg/1)
Marketing started19961231
Package count4

External sources

Source: openFDA. Public-domain (CC0).