Dilantin is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Parke-davis Div Of Pfizer Inc. The primary component is Phenytoin Sodium.
Product ID | 0071-0369_06311c9f-47af-4aae-a7a4-a0a40182ee7c |
NDC | 0071-0369 |
Product Type | Human Prescription Drug |
Proprietary Name | Dilantin |
Generic Name | Extended Phenytoin Sodium |
Dosage Form | Capsule |
Route of Administration | ORAL |
Marketing Start Date | 1976-08-27 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA084349 |
Labeler Name | Parke-Davis Div of Pfizer Inc |
Substance Name | PHENYTOIN SODIUM |
Active Ingredient Strength | 100 mg/1 |
Pharm Classes | Anti-epileptic Agent [EPC], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 1976-08-27 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA084349 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1976-08-27 |
Marketing Category | ANDA |
Application Number | ANDA084349 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1976-08-27 |
Marketing Category | ANDA |
Application Number | ANDA084349 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1976-08-27 |
Ingredient | Strength |
---|---|
PHENYTOIN SODIUM | 100 mg/1 |
SPL SET ID: | 8848de76-8d74-4620-bcc7-a86a596e5dd9 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0071-0369 | Dilantin | Extended Phenytoin Sodium |
0071-3740 | Dilantin | Extended Phenytoin Sodium |
43353-131 | Dilantin | Phenytoin Sodium |
50090-0029 | Dilantin | Phenytoin Sodium |
68151-1019 | Dilantin | Phenytoin Sodium |
69189-3742 | Dilantin | Phenytoin Sodium |
70518-0980 | Dilantin | Phenytoin Sodium |
55289-906 | EXTENDED PHENYTOIN SODIUM | EXTENDED PHENYTOIN SODIUM |
55648-720 | EXTENDED PHENYTOIN SODIUM | EXTENDED PHENYTOIN SODIUM |
64679-720 | EXTENDED PHENYTOIN SODIUM | EXTENDED PHENYTOIN SODIUM |
64725-0720 | EXTENDED PHENYTOIN SODIUM | EXTENDED PHENYTOIN SODIUM |
68180-561 | Extended Phenytoin Sodium | Extended Phenytoin Sodium |
0378-2670 | Phenytek | extended phenytoin sodium |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DILANTIN 71404865 0359292 Live/Registered |
PARKE, DAVIS & COMPANY 1938-04-04 |