FDA NDC Directory · JSON-LD · Markdown

Ranitidine

NDC 55111-404 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078192
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsRANITIDINE HYDROCHLORIDE (150 mg/1)
Marketing started20091202
Package count14

External sources

Source: openFDA. Public-domain (CC0).