# Misoprostol

NDC: 82804-037
Generic name: Misoprostol
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220411

FDA application: ANDA076095

## Active ingredients

- MISOPROSTOL: 200 ug/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82804-037"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-037
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=85410e16-d164-4666-9539-778e2b4dd138