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Ranitidine

NDC 62207-773 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerGranules India Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA210243
Dosage form / routeTABLET · ORAL
Active ingredientsRANITIDINE HYDROCHLORIDE (150 mg/1)
Marketing started20190626
Package count4

External sources

Source: openFDA. Public-domain (CC0).