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Amitriptyline Hydrochloride

NDC 69367-388 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212654
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsAMITRIPTYLINE HYDROCHLORIDE (10 mg/1)
Marketing started20240520
Package count2

External sources

Source: openFDA. Public-domain (CC0).