# MISOPROSTOL

NDC: 42571-253
Generic name: Misoprostol
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230101

FDA application: ANDA216872

## Active ingredients

- MISOPROSTOL: 100 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42571-253"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-253
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=54d26ca3-d309-4048-8699-a04b3854ef9c