United States · FDA National Drug Code directory
Heparin Sodium
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
- 76045-108_fb5b2c56-f5ea-42c9-a6d8-37a03770290b
- Product NDC
- 76045-108
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Heparin Sodium
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160610
- Source listing expiry
- 20261231
Source-listed ingredients
- HEPARIN SODIUM — 5000 [USP'U]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 24 BLISTER PACK in 1 CARTON (76045-108-10) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-108-00) / 1 mL in 1 SYRINGE, GLASS · 76045-108-10
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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