# Sulfameth/Trimeth-DS

NDC: 61919-645
Generic name: Sulfameth/Trimeth-DS
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190813

FDA application: ANDA090624

## Active ingredients

- SULFAMETHOXAZOLE: 800 mg/1
- TRIMETHOPRIM: 160 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"61919-645"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61919-645
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=90026ce8-3305-6272-e053-2995a90a57e0