# carboprost tromethamine

NDC: 70069-825
Generic name: carboprost tromethamine
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 20260605

FDA application: ANDA219529

## Active ingredients

- CARBOPROST TROMETHAMINE: 250 ug/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-825"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-825
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d79f4342-2d37-4a47-958e-ab800d4f3918
