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PHENYTOIN SODIUM
PHENYTOIN SODIUM - 62756-402-03 - (PHENYTOIN SODIUM)
Drug Information of PHENYTOIN SODIUM
| Product NDC: | 62756-402 |
| 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: | 62756-402 |
| Labeler Name: | SUN PHARMACEUTICAL INDUSTRIES LIMITED |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040621 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20061212 |
Package Information of PHENYTOIN SODIUM
| Package NDC: | 62756-402-03 |
| Package Description: | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-402-03) |
NDC Information of PHENYTOIN SODIUM
| NDC Code | 62756-402-03 |
| Proprietary Name | PHENYTOIN SODIUM |
| Package Description | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-402-03) |
| Product NDC | 62756-402 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PHENYTOIN SODIUM |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20061212 |
| Marketing Category Name | ANDA |
| Labeler Name | SUN PHARMACEUTICAL INDUSTRIES LIMITED |
| 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] |
