# Diclofenac Sodium/Misoprostol DICLOFENAC-SODIUM-MISOPROSTOL

NDC: 42571-133
Generic name: Diclofenac Sodium/Misoprostol
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210901

FDA application: ANDA204355

## Active ingredients

- DICLOFENAC SODIUM: 50 mg/1
- MISOPROSTOL: 200 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42571-133"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-133
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c61df58d-d6bb-4d3e-9ef8-60caa7d4e762