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Phenytoin
Phenytoin - 0472-5002-08 - (Phenytoin)
Drug Information of Phenytoin
| Product NDC: | 0472-5002 |
| Proprietary Name: | Phenytoin |
| Non Proprietary Name: | Phenytoin |
| Active Ingredient(s): | 125 mg/5mL & nbsp; Phenytoin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Phenytoin
| Product NDC: | 0472-5002 |
| Labeler Name: | Actavis Mid Atlantic LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089892 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090302 |
Package Information of Phenytoin
| Package NDC: | 0472-5002-08 |
| Package Description: | 237 mL in 1 BOTTLE (0472-5002-08) |
NDC Information of Phenytoin
| NDC Code | 0472-5002-08 |
| Proprietary Name | Phenytoin |
| Package Description | 237 mL in 1 BOTTLE (0472-5002-08) |
| Product NDC | 0472-5002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenytoin |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20090302 |
| Marketing Category Name | ANDA |
| Labeler Name | Actavis Mid Atlantic LLC |
| Substance Name | PHENYTOIN |
| Strength Number | 125 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
