FDA NDC Directory · JSON-LD · Markdown

Nortriptyline Hydrochloride

NDC 51672-4002 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075520
Dosage form / routeCAPSULE · ORAL
Active ingredientsNORTRIPTYLINE HYDROCHLORIDE (25 mg/1)
Marketing started20000508
Package count5

External sources

Source: openFDA. Public-domain (CC0).