FDA NDC Directory · JSON-LD · Markdown

Amitriptyline Hydrochloride

NDC 16571-105 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217411
Dosage form / routeTABLET · ORAL
Active ingredientsAMITRIPTYLINE HYDROCHLORIDE (10 mg/1)
Marketing started20230610
Package count2

External sources

Source: openFDA. Public-domain (CC0).