# carboprost tromethamine

NDC: 70512-859
Generic name: carboprost tromethamine
Labeler / Manufacturer: SOLA Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 20230925

FDA application: ANDA216824

## Active ingredients

- CARBOPROST TROMETHAMINE: 250 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70512-859"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70512-859
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=32cb34f5-e199-4cf8-a848-aaec7d42bd10