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Heparin Sodium in Sodium Chloride
Heparin Sodium in Sodium Chloride - 0264-9872-10 - (Heparin Sodium in Sodium Chloride)
Drug Information of Heparin Sodium in Sodium Chloride
| Product NDC: | 0264-9872 |
| Proprietary Name: | Heparin Sodium in Sodium Chloride |
| Non Proprietary Name: | Heparin Sodium in Sodium Chloride |
| Active Ingredient(s): | 200 [USP'U]/100mL & nbsp; Heparin Sodium in Sodium Chloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Heparin Sodium in Sodium Chloride
| Product NDC: | 0264-9872 |
| Labeler Name: | B. Braun Medical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019953 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19920720 |
Package Information of Heparin Sodium in Sodium Chloride
| Package NDC: | 0264-9872-10 |
| Package Description: | 24 CONTAINER in 1 CASE (0264-9872-10) > 500 mL in 1 CONTAINER |
NDC Information of Heparin Sodium in Sodium Chloride
| NDC Code | 0264-9872-10 |
| Proprietary Name | Heparin Sodium in Sodium Chloride |
| Package Description | 24 CONTAINER in 1 CASE (0264-9872-10) > 500 mL in 1 CONTAINER |
| Product NDC | 0264-9872 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Heparin Sodium in Sodium Chloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19920720 |
| Marketing Category Name | NDA |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | HEPARIN SODIUM |
| Strength Number | 200 |
| Strength Unit | [USP'U]/100mL |
| Pharmaceutical Classes | Anti-coagulant [EPC],Heparin [Chemical/Ingredient],Unfractionated Heparin [EPC] |
