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EXTENDED PHENYTOIN SODIUM
EXTENDED PHENYTOIN SODIUM - 55289-906-60 - (EXTENDED PHENYTOIN SODIUM)
Drug Information of EXTENDED PHENYTOIN SODIUM
| Product NDC: | 55289-906 |
| 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: | 55289-906 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040732 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080130 |
Package Information of EXTENDED PHENYTOIN SODIUM
| Package NDC: | 55289-906-60 |
| Package Description: | 60 CAPSULE in 1 BOTTLE, PLASTIC (55289-906-60) |
NDC Information of EXTENDED PHENYTOIN SODIUM
| NDC Code | 55289-906-60 |
| Proprietary Name | EXTENDED PHENYTOIN SODIUM |
| Package Description | 60 CAPSULE in 1 BOTTLE, PLASTIC (55289-906-60) |
| Product NDC | 55289-906 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | EXTENDED PHENYTOIN SODIUM |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20080130 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, 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] |
