# Cefaclor

NDC: 81948-6250
Generic name: cefaclor
Labeler / Manufacturer: Azorian Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20221101

FDA application: ANDA065412

## Active ingredients

- CEFACLOR: 250 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81948-6250"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81948-6250
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=224af904-38f3-4210-a750-e21006db4c66