# Ranitidine

NDC: 53746-253
Generic name: Ranitidine
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20091216

FDA application: ANDA077824

## Active ingredients

- RANITIDINE HYDROCHLORIDE: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"53746-253"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53746-253
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b38a3332-5c54-453f-aeb7-070f830955c2