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Dilantin Infatabs
Dilantin Infatabs - 55154-2416-0 - (Phenytoin)
Drug Information of Dilantin Infatabs
| Product NDC: | 55154-2416 |
| Proprietary Name: | Dilantin Infatabs |
| 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 Dilantin Infatabs
| Product NDC: | 55154-2416 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084427 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19790226 |
Package Information of Dilantin Infatabs
| Package NDC: | 55154-2416-0 |
| Package Description: | 10 BLISTER PACK in 1 BAG (55154-2416-0) > 1 TABLET, CHEWABLE in 1 BLISTER PACK |
NDC Information of Dilantin Infatabs
| NDC Code | 55154-2416-0 |
| Proprietary Name | Dilantin Infatabs |
| Package Description | 10 BLISTER PACK in 1 BAG (55154-2416-0) > 1 TABLET, CHEWABLE in 1 BLISTER PACK |
| Product NDC | 55154-2416 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Phenytoin |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 19790226 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | PHENYTOIN |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE] |
