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Phenytoin Sodium
Phenytoin Sodium - 51672-4111-0 - (Phenytoin Sodium)
Drug Information of Phenytoin Sodium
| Product NDC: | 51672-4111 |
| Proprietary Name: | Phenytoin Sodium |
| Non Proprietary Name: | Phenytoin Sodium |
| Active Ingredient(s): | 100 mg/1 & nbsp; Phenytoin Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenytoin Sodium
| Product NDC: | 51672-4111 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040684 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060905 |
Package Information of Phenytoin Sodium
| Package NDC: | 51672-4111-0 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (51672-4111-0) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Phenytoin Sodium
| NDC Code | 51672-4111-0 |
| Proprietary Name | Phenytoin Sodium |
| Package Description | 10 BLISTER PACK in 1 CARTON (51672-4111-0) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 51672-4111 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenytoin Sodium |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20060905 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | PHENYTOIN SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
