NDC 71839-117 – Heparin Sodium
Heparin Sodium 2000 [USP'U]/2mL · Injection, Solution · Intravenous, Subcutaneous
Product NDC71839-117
Product details
- Brand name
- Heparin Sodium
- Generic name
- Heparin Sodium
- Labeler
- BE Pharmaceuticals Inc.
- Dosage form
- Injection, Solution
- Route
- Intravenous, Subcutaneous
- Marketing category
- ANDA · ANDA214804
- Marketed since
- December 29, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-coagulant; Unfractionated Heparin
Active ingredients
- Heparin Sodium 2000 [USP'U]/2mL
Uses, dosage, side effects and warnings for Heparin Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 71839-117-25 | 25 VIAL, SINGLE-DOSE in 1 CARTON (71839-117-25) / 2 mL in 1 VIAL, SINGLE-DOSE (71839-117-01) | Dec 29, 2020 |
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