Home
>
National Drug Code (NDC)
>
EXTENDED PHENYTOIN SODIUM
EXTENDED PHENYTOIN SODIUM - 49349-471-51 - (EXTENDED PHENYTOIN SODIUM)
Drug Information of EXTENDED PHENYTOIN SODIUM
| Product NDC: | 49349-471 |
| Proprietary Name: | EXTENDED PHENYTOIN SODIUM |
| Non Proprietary Name: | EXTENDED PHENYTOIN SODIUM |
| Active Ingredient(s): | 100 mg/1 & nbsp; EXTENDED PHENYTOIN SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EXTENDED PHENYTOIN SODIUM
| Product NDC: | 49349-471 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040732 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130409 |
Package Information of EXTENDED PHENYTOIN SODIUM
| Package NDC: | 49349-471-51 |
| Package Description: | 9 CAPSULE in 1 BLISTER PACK (49349-471-51) |
NDC Information of EXTENDED PHENYTOIN SODIUM
| NDC Code | 49349-471-51 |
| Proprietary Name | EXTENDED PHENYTOIN SODIUM |
| Package Description | 9 CAPSULE in 1 BLISTER PACK (49349-471-51) |
| Product NDC | 49349-471 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | EXTENDED PHENYTOIN SODIUM |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130409 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK 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] |
