Heparin Sodium in Dextrose is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by B. Braun Medical Inc.. The primary component is Heparin Sodium; Dextrose Monohydrate.
| Product ID | 0264-9567_28259cc2-7b2f-41ab-9d80-da4c6ae01280 |
| NDC | 0264-9567 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Heparin Sodium in Dextrose |
| Generic Name | Heparin Sodium And Dextrose |
| Dosage Form | Injection |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 1992-07-20 |
| Marketing Category | NDA / NDA |
| Application Number | NDA019952 |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | HEPARIN SODIUM; DEXTROSE MONOHYDRATE |
| Active Ingredient Strength | 4000 [USP'U]/100mL; g/100mL |
| Pharm Classes | Anti-coagulant [EPC],Heparin [CS],Unfractionated Heparin [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 1992-07-20 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA019952 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1992-07-20 |
| Ingredient | Strength |
|---|---|
| HEPARIN SODIUM | 4000 [USP'U]/100mL |
| SPL SET ID: | 92a6f533-1a3d-4734-b413-d245592454e3 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0264-9567 | Heparin Sodium in Dextrose | Heparin Sodium and Dextrose |
| 0264-9577 | Heparin Sodium in Dextrose | Heparin Sodium and Dextrose |
| 0264-9587 | Heparin Sodium in Dextrose | Heparin Sodium and Dextrose |
| 50090-4537 | Heparin Sodium in Dextrose | Heparin Sodium and Dextrose |