FDA NDC Directory · JSON-LD · Markdown

RANITIDINE

NDC 71993-314 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAtland Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211289
Dosage form / routeTABLET · ORAL
Active ingredientsRANITIDINE HYDROCHLORIDE (150 mg/1)
Marketing started20260918
Package count1

External sources

Source: openFDA. Public-domain (CC0).