# Ranitidine

NDC: 55111-404
Generic name: Ranitidine
Labeler / Manufacturer: Dr. Reddy's Laboratories Limited
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20091202

FDA application: ANDA078192

## 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:"55111-404"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-404
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=00df8a42-296f-80dd-98af-ee8b30eb38cc