# Cefepime

NDC: 63323-340
Generic name: Cefepime
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20100830

FDA application: ANDA065441

## Active ingredients

- CEFEPIME HYDROCHLORIDE: 2 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-340"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-340
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5e1695e0-1310-4cd8-a5da-ad1a7dcd1792