# Cefepime Hydrochloride

NDC: 0143-9382
Generic name: Cefepime Hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20250922

FDA application: ANDA214402

## Active ingredients

- CEFEPIME HYDROCHLORIDE: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9382"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9382
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b9914e7e-13f6-42d4-9cbb-8c7ed1ce7a01