United States · FDA National Drug Code directory
CARBOPROST TROMETHAMINE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 81665-202_4cded8b1-0f1c-219d-e063-6294a90a64e2
- Product NDC
- 81665-202
- Form
- INJECTION, SOLUTION
- Composition / generic term
- carboprost tromethamine
- Labeler
- Omnivium Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250515
- Source listing expiry
- 20271231
Source-listed ingredients
- CARBOPROST TROMETHAMINE — 250 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 mL in 1 AMPULE (81665-202-01) · 81665-202-01
- 10 AMPULE in 1 CARTON (81665-202-10) / 1 mL in 1 AMPULE (81665-202-01) · 81665-202-10
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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