# Cefepime

NDC: 0409-9566
Generic name: Cefepime
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20200824

FDA application: ANDA065441

## 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:"0409-9566"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-9566
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e80c27e2-164d-4836-ba24-c160d75dc5d3