# Cefotan

NDC: 0121-0976
Generic name: Cefotetan
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20240408

FDA application: NDA050588

## Active ingredients

- CEFOTETAN DISODIUM: 1 g/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-0976"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-0976
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f1510f5e-d001-44e0-accb-27cf79fd4f9a