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PHENYTOIN
PHENYTOIN - 16590-815-82 - (PHENYTOIN SODIUM)
Drug Information of PHENYTOIN
| Product NDC: | 16590-815 |
| Proprietary Name: | PHENYTOIN |
| Non Proprietary Name: | PHENYTOIN SODIUM |
| Active Ingredient(s): | 100 mg/1 & nbsp; PHENYTOIN SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PHENYTOIN
| Product NDC: | 16590-815 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040298 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091120 |
Package Information of PHENYTOIN
| Package NDC: | 16590-815-82 |
| Package Description: | 180 CAPSULE in 1 BOTTLE, PLASTIC (16590-815-82) |
NDC Information of PHENYTOIN
| NDC Code | 16590-815-82 |
| Proprietary Name | PHENYTOIN |
| Package Description | 180 CAPSULE in 1 BOTTLE, PLASTIC (16590-815-82) |
| Product NDC | 16590-815 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PHENYTOIN SODIUM |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20091120 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| 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] |
