# SULFADIAZINE

NDC: 42806-757
Generic name: sulfadiazine
Labeler / Manufacturer: EPIC PHARMA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20211215

FDA application: ANDA040091

## Active ingredients

- SULFADIAZINE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42806-757"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42806-757
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8993651b-fff6-4e3f-9b60-78587bc9bcee