# Cefdinir

NDC: 0093-4136
Generic name: Cefdinir
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20070508

FDA application: ANDA065332

## Active ingredients

- CEFDINIR MONOHYDRATE: 125 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-4136"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-4136
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a1f49fe1-b511-4f6b-a912-8ae8662d95a5