# Cefepime

NDC: 67184-1002
Generic name: CEFEPIME HYDROCHLORIDE
Labeler / Manufacturer: Qilu Pharmaceutical Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20160201

FDA application: ANDA203704

## Active ingredients

- CEFEPIME HYDROCHLORIDE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67184-1002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67184-1002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=80b4c811-4a71-47fb-8565-85ce9d0f782c