FDA NDC Directory · JSON-LD · Markdown

Nortriptyline Hydrochloride

NDC 70710-1155 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213441
Dosage form / routeCAPSULE · ORAL
Active ingredientsNORTRIPTYLINE HYDROCHLORIDE (50 mg/1)
Marketing started20220210
Package count3

External sources

Source: openFDA. Public-domain (CC0).