# Famotidine

NDC: 0641-6022
Generic name: Famotidine
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20010416

FDA application: ANDA075486

## Active ingredients

- FAMOTIDINE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0641-6022"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6022
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1fdf16e5-145d-4c19-a318-fc6c10794b50