# Misoprostol

NDC: 43386-161
Generic name: Misoprostol
Labeler / Manufacturer: Lupin Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20120725

FDA application: ANDA091667

## Active ingredients

- MISOPROSTOL: 200 ug/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43386-161"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43386-161
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=14f73ae3-7d8d-4d10-b668-8bd5adf8032c