# FAMOTIDINE

NDC: 72205-233
Generic name: FAMOTIDINE
Labeler / Manufacturer: Novadoz Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20250724

FDA application: ANDA219863

## Active ingredients

- FAMOTIDINE: 40 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72205-233"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72205-233
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=21953598-e7ec-45c2-8fca-05550a1ddf38