Home
>
National Drug Code (NDC)
>
Phenytoin
Phenytoin - 17856-0067-3 - (Phenytoin)
Drug Information of Phenytoin
| Product NDC: | 17856-0067 |
| 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: | 17856-0067 |
| Labeler Name: | Atlantic Biologicals Corps |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040420 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020624 |
Package Information of Phenytoin
| Package NDC: | 17856-0067-3 |
| Package Description: | 4 mL in 1 CUP (17856-0067-3) |
NDC Information of Phenytoin
| NDC Code | 17856-0067-3 |
| Proprietary Name | Phenytoin |
| Package Description | 4 mL in 1 CUP (17856-0067-3) |
| Product NDC | 17856-0067 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenytoin |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20020624 |
| Marketing Category Name | ANDA |
| Labeler Name | Atlantic Biologicals Corps |
| Substance Name | PHENYTOIN |
| Strength Number | 125 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
