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Fosphenytoin Sodium
Fosphenytoin Sodium - 47335-834-01 - (Fosphenytoin Sodium)
Drug Information of Fosphenytoin Sodium
| Product NDC: | 47335-834 |
| Proprietary Name: | Fosphenytoin Sodium |
| Non Proprietary Name: | Fosphenytoin Sodium |
| Active Ingredient(s): | 50 mg/mL & nbsp; Fosphenytoin Sodium |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fosphenytoin Sodium
| Product NDC: | 47335-834 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078417 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090814 |
Package Information of Fosphenytoin Sodium
| Package NDC: | 47335-834-01 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (47335-834-01) > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Fosphenytoin Sodium
| NDC Code | 47335-834-01 |
| Proprietary Name | Fosphenytoin Sodium |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (47335-834-01) > 10 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 47335-834 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fosphenytoin Sodium |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20090814 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | FOSPHENYTOIN SODIUM |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
