FDA NDC Directory · JSON-LD · Markdown

TRAMADOL HYDROCHLORIDE

NDC 47335-860 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201384
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsTRAMADOL HYDROCHLORIDE (200 mg/1)
Marketing started20111212
Package count4

External sources

Source: openFDA. Public-domain (CC0).