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Phenytoin Sodium
Phenytoin Sodium - 51079-905-19 - (phenytoin sodium)
Drug Information of Phenytoin Sodium
| Product NDC: | 51079-905 |
| 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: | 51079-905 |
| Labeler Name: | Mylan Institutional Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040298 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120912 |
Package Information of Phenytoin Sodium
| Package NDC: | 51079-905-19 |
| Package Description: | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-905-19) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (51079-905-17) |
NDC Information of Phenytoin Sodium
| NDC Code | 51079-905-19 |
| Proprietary Name | Phenytoin Sodium |
| Package Description | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-905-19) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (51079-905-17) |
| Product NDC | 51079-905 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | phenytoin sodium |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120912 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional 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] |
