# Ranitidine

NDC: 0121-0727
Generic name: RANITIDINE
Labeler / Manufacturer: Pharmaceutical Associates, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SYRUP
Routes: ORAL
Marketing started: 20101101

FDA application: ANDA077405

## Active ingredients

- RANITIDINE: 15 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-0727"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-0727
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d0da9dd6-c691-4614-99c7-531b0bf34837