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
- 71839-117_4d2cbee1-f461-45a1-bf5f-c8dd4ef8501b
- Product NDC
- 71839-117
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Heparin Sodium
- Labeler
- BE Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201229
- Source listing expiry
- 20261231
Source-listed ingredients
- HEPARIN SODIUM — 2000 [USP'U]/2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, SINGLE-DOSE in 1 CARTON (71839-117-25) / 2 mL in 1 VIAL, SINGLE-DOSE (71839-117-01) · 71839-117-25
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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