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Phenytoin Sodium
Phenytoin Sodium - 0409-1317-01 - (PHENYTOIN SODIUM)
Drug Information of Phenytoin Sodium
| Product NDC: | 0409-1317 |
| Proprietary Name: | Phenytoin Sodium |
| Non Proprietary Name: | PHENYTOIN SODIUM |
| Active Ingredient(s): | 50 mg/mL & nbsp; PHENYTOIN SODIUM |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenytoin Sodium
| Product NDC: | 0409-1317 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089521 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110217 |
Package Information of Phenytoin Sodium
| Package NDC: | 0409-1317-01 |
| Package Description: | 5 TRAY in 1 CONTAINER (0409-1317-01) > 5 AMPULE in 1 TRAY > 2 mL in 1 AMPULE |
NDC Information of Phenytoin Sodium
| NDC Code | 0409-1317-01 |
| Proprietary Name | Phenytoin Sodium |
| Package Description | 5 TRAY in 1 CONTAINER (0409-1317-01) > 5 AMPULE in 1 TRAY > 2 mL in 1 AMPULE |
| Product NDC | 0409-1317 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PHENYTOIN SODIUM |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20110217 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | PHENYTOIN SODIUM |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
