# Cephalexin

NDC: 68071-2889
Generic name: Cephalexin
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: FOR SUSPENSION
Routes: ORAL
Marketing started: 20190328

FDA application: ANDA210221

## Active ingredients

- CEPHALEXIN: 250 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-2889"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-2889
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ee278959-d321-d356-e053-2995a90a32c2