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Amitriptyline Hydrochloride

NDC 29300-421 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerUnichem Pharmaceuticals (USA), Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214548
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMITRIPTYLINE HYDROCHLORIDE (50 mg/1)
Marketing started20210526
Package count3

External sources

Source: openFDA. Public-domain (CC0).