# Sulfamethoxazole and Trimethoprim

NDC: 0121-0853
Generic name: Sulfamethoxazole and Trimethoprim
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20240805

FDA application: NDA018615

## Active ingredients

- SULFAMETHOXAZOLE: 200 mg/5mL
- TRIMETHOPRIM: 40 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-0853"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-0853
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=777da85a-a776-4681-976d-326ec421cfc9