Heparin Sodium 00781-3555
Product NDC
00781-3555- Manufacturer
- Sandoz Inc.
- Dosage Form
- Injection, Solution
- Route
- Intravenous And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- June 12, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA202732
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Heparin Sodium | 1000 [USP'U]/mL |
Drug Class
Anti-coagulant [EPC]Heparin [CS]Unfractionated Heparin [EPC]
Packaging Options(1)
25 VIAL, SINGLE-DOSE in 1 CARTON (0781-3555-25) / 2 mL in 1 VIAL, SINGLE-DOSE (0781-3555-10)