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Amitriptyline Hydrochloride

NDC 57664-690 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA089399
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMITRIPTYLINE HYDROCHLORIDE (100 mg/1)
Marketing started19870714
Package count1

External sources

Source: openFDA. Public-domain (CC0).