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fomepizole
fomepizole - 0781-3182-84 - (fomepizole)
Drug Information of fomepizole
| Product NDC: | 0781-3182 |
| Proprietary Name: | fomepizole |
| Non Proprietary Name: | fomepizole |
| Active Ingredient(s): | 1 g/mL & nbsp; fomepizole |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of fomepizole
| Product NDC: | 0781-3182 |
| Labeler Name: | Sandoz Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078537 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080306 |
Package Information of fomepizole
| Package NDC: | 0781-3182-84 |
| Package Description: | 4 CARTON in 1 CARTON (0781-3182-84) > 1 VIAL in 1 CARTON (0781-3182-73) > 1.5 mL in 1 VIAL |
NDC Information of fomepizole
| NDC Code | 0781-3182-84 |
| Proprietary Name | fomepizole |
| Package Description | 4 CARTON in 1 CARTON (0781-3182-84) > 1 VIAL in 1 CARTON (0781-3182-73) > 1.5 mL in 1 VIAL |
| Product NDC | 0781-3182 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fomepizole |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080306 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc. |
| Substance Name | FOMEPIZOLE |
| Strength Number | 1 |
| Strength Unit | g/mL |
| Pharmaceutical Classes | Antidote [EPC] |
