# CARBOPROST TROMETHAMINE

NDC: 71839-137
Generic name: carboprost tromethamine
Labeler / Manufacturer: BE Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR
Marketing started: 20230511

FDA application: ANDA216882

## 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:"71839-137"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71839-137
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8447d4f1-d286-4aa0-a379-a673518da045