# RANITIDINE

NDC: 71993-314
Generic name: RANITIDINE
Labeler / Manufacturer: Atland Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260918

FDA application: ANDA211289

## 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:"71993-314"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71993-314