# CARBOPROST TROMETHAMINE

NDC: 81665-202
Generic name: carboprost tromethamine
Labeler / Manufacturer: Omnivium Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 20250515

FDA application: ANDA213118

## 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:"81665-202"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81665-202