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Phenytoin
Phenytoin - 0378-3850-01 - (Phenytoin)
Drug Information of Phenytoin
| Product NDC: | 0378-3850 |
| Proprietary Name: | Phenytoin |
| Non Proprietary Name: | Phenytoin |
| Active Ingredient(s): | 50 mg/1 & nbsp; Phenytoin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenytoin
| Product NDC: | 0378-3850 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200691 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121226 |
Package Information of Phenytoin
| Package NDC: | 0378-3850-01 |
| Package Description: | 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0378-3850-01) |
NDC Information of Phenytoin
| NDC Code | 0378-3850-01 |
| Proprietary Name | Phenytoin |
| Package Description | 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0378-3850-01) |
| Product NDC | 0378-3850 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenytoin |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20121226 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | PHENYTOIN |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
