# Misoprostol

NDC: 54348-148
Generic name: MISOPROSTOL
Labeler / Manufacturer: PharmPak, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190710

FDA application: ANDA091667

## 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:"54348-148"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54348-148
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b07b3dfc-1cb5-484c-be11-8d14c89c794f