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Chlordiazepoxide and Amitriptyline Hydrochloride

NDC 42571-302 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA211925
Dosage form / routeTABLET · ORAL
Active ingredientsAMITRIPTYLINE HYDROCHLORIDE (5 mg/1)
CHLORDIAZEPOXIDE (12.5 mg/1)
Marketing started20220401
Package count2

External sources

Source: openFDA. Public-domain (CC0).