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Amitriptyline Hydrochloride

NDC 70518-4366 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA212654
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsAMITRIPTYLINE HYDROCHLORIDE (100 mg/1)
Marketing started20250619
Package count1

External sources

Source: openFDA. Public-domain (CC0).