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Flumazenil
Flumazenil - 25021-600-05 - (flumazenil)
Drug Information of Flumazenil
| Product NDC: | 25021-600 |
| 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: | 25021-600 |
| Labeler Name: | Sagent Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090584 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120915 |
Package Information of Flumazenil
| Package NDC: | 25021-600-05 |
| Package Description: | 10 VIAL in 1 CARTON (25021-600-05) > 5 mL in 1 VIAL |
NDC Information of Flumazenil
| NDC Code | 25021-600-05 |
| Proprietary Name | Flumazenil |
| Package Description | 10 VIAL in 1 CARTON (25021-600-05) > 5 mL in 1 VIAL |
| Product NDC | 25021-600 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | flumazenil |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120915 |
| Marketing Category Name | ANDA |
| Labeler Name | Sagent Pharmaceuticals |
| Substance Name | FLUMAZENIL |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine Antagonist [EPC] |
