FDA NDC Directory · JSON-LD · Markdown

TRAMADOL HYDROCHLORIDE

NDC 71205-656 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA201384
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsTRAMADOL HYDROCHLORIDE (300 mg/1)
Marketing started20111212
Package count3

External sources

Source: openFDA. Public-domain (CC0).