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Protriptyline Hydrochloride

NDC 42794-007 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSigmapharm Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090462
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPROTRIPTYLINE HYDROCHLORIDE (10 mg/1)
Marketing started20200302
Package count1

External sources

Source: openFDA. Public-domain (CC0).