Heparin Sodium 87188-0102
Product NDC
87188-0102- Manufacturer
- Plano Pharmaceuticals Inc.
- Dosage Form
- Injection
- Route
- Intravenous And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- June 8, 2011
- Listing Expires
- December 31, 2027
- Application
- ANDA091682
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Heparin Sodium | 5000 [USP'U]/mL |
Drug Class
Anti-coagulant [EPC]Heparin [CS]Unfractionated Heparin [EPC]
Packaging Options(1)
25 VIAL, MULTI-DOSE in 1 CARTON (87188-102-90) / 1 mL in 1 VIAL, MULTI-DOSE (87188-102-01)