FDA NDC Directory · JSON-LD · Markdown

Ranitidine

NDC 55111-131 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA075294
Dosage form / routeTABLET · ORAL
Active ingredientsRANITIDINE HYDROCHLORIDE (75 mg/1)
Marketing started20000301
Package count10

External sources

Source: openFDA. Public-domain (CC0).