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Amitriptyline Hydrochloride

NDC 60760-686 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerST. MARY'S MEDICAL PARK PHARMACY
Marketing categoryAbbreviated NDA (generic) · App ANDA217411
Dosage form / routeTABLET · ORAL
Active ingredientsAMITRIPTYLINE HYDROCHLORIDE (50 mg/1)
Marketing started20230610
Package count1

External sources

Source: openFDA. Public-domain (CC0).