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Fosphenytoin Sodium
Fosphenytoin Sodium - 0143-9704-25 - (Fosphenytoin Sodium)
Drug Information of Fosphenytoin Sodium
| Product NDC: | 0143-9704 |
| Proprietary Name: | Fosphenytoin Sodium |
| Non Proprietary Name: | Fosphenytoin Sodium |
| Active Ingredient(s): | 50 mg/mL & nbsp; Fosphenytoin Sodium |
| Administration Route(s): | INTRAMUSCULAR; INTRAVASCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fosphenytoin Sodium
| Product NDC: | 0143-9704 |
| Labeler Name: | West-Ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078765 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091202 |
Package Information of Fosphenytoin Sodium
| Package NDC: | 0143-9704-25 |
| Package Description: | 25 VIAL in 1 PACKAGE (0143-9704-25) > 2 mL in 1 VIAL (0143-9704-01) |
NDC Information of Fosphenytoin Sodium
| NDC Code | 0143-9704-25 |
| Proprietary Name | Fosphenytoin Sodium |
| Package Description | 25 VIAL in 1 PACKAGE (0143-9704-25) > 2 mL in 1 VIAL (0143-9704-01) |
| Product NDC | 0143-9704 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fosphenytoin Sodium |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVASCULAR |
| Start Marketing Date | 20091202 |
| Marketing Category Name | ANDA |
| Labeler Name | West-Ward Pharmaceutical Corp |
| 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] |
