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Amitriptyline Hydrochloride

NDC 70756-201 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLifestar Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213999
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMITRIPTYLINE HYDROCHLORIDE (10 mg/1)
Marketing started20210223
Package count2

External sources

Source: openFDA. Public-domain (CC0).