FDA NDC Directory · JSON-LD · Markdown

Tramadol Hydrochloride

NDC 68180-383 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200503
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsTRAMADOL HYDROCHLORIDE (100 mg/1)
Marketing started20110926
Package count0

External sources

Source: openFDA. Public-domain (CC0).