United States · FDA National Drug Code directory
Cosyntropin
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
- 0781-3440_7e07a53d-7214-4471-859f-059d66318106
- Product NDC
- 0781-3440
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Cosyntropin
- Labeler
- Sandoz Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120629
- Source listing expiry
- 20261231
Source-listed ingredients
- COSYNTROPIN — .25 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (0781-3440-95) / 1 mL in 1 VIAL (0781-3440-71) · 0781-3440-95
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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