Heparin Sodium 00409-2222
Product NDC
00409-2222- Manufacturer
- Hospira, Inc.
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- February 27, 2023
- Listing Expires
- December 31, 2027
- Application
- NDA018916
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Heparin Sodium | 200 [USP'U]/100mL |
Drug Class
Anti-coagulant [EPC]Heparin [CS]Unfractionated Heparin [EPC]
Packaging Options(1)
12 POUCH in 1 CASE (0409-2222-12) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG (0409-2222-01)