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Flumazenil
Flumazenil - 10019-321-02 - (Flumazenil)
Drug Information of Flumazenil
| Product NDC: | 10019-321 |
| Proprietary Name: | Flumazenil |
| Non Proprietary Name: | Flumazenil |
| Active Ingredient(s): | .1 mg/mL & nbsp; Flumazenil |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flumazenil
| Product NDC: | 10019-321 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076787 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100526 |
Package Information of Flumazenil
| Package NDC: | 10019-321-02 |
| Package Description: | 10 VIAL, MULTI-DOSE in 1 PACKAGE (10019-321-02) > 10 mL in 1 VIAL, MULTI-DOSE (10019-321-62) |
NDC Information of Flumazenil
| NDC Code | 10019-321-02 |
| Proprietary Name | Flumazenil |
| Package Description | 10 VIAL, MULTI-DOSE in 1 PACKAGE (10019-321-02) > 10 mL in 1 VIAL, MULTI-DOSE (10019-321-62) |
| Product NDC | 10019-321 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flumazenil |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100526 |
| Marketing Category Name | ANDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | FLUMAZENIL |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine Antagonist [EPC] |
