Dilantin - 0071-0369-40 - (PHENYTOIN SODIUM)

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Drug Information of Dilantin

Product NDC: 0071-0369
Proprietary Name: Dilantin
Non Proprietary Name: PHENYTOIN SODIUM
Active Ingredient(s): 100    mg/1 & nbsp;   PHENYTOIN SODIUM
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Dilantin

Product NDC: 0071-0369
Labeler Name: Parke-Davis Div of Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084349
Marketing Category: ANDA
Start Marketing Date: 19760827

Package Information of Dilantin

Package NDC: 0071-0369-40
Package Description: 100 BLISTER PACK in 1 CARTON (0071-0369-40) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Dilantin

NDC Code 0071-0369-40
Proprietary Name Dilantin
Package Description 100 BLISTER PACK in 1 CARTON (0071-0369-40) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 0071-0369
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PHENYTOIN SODIUM
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19760827
Marketing Category Name ANDA
Labeler Name Parke-Davis Div of Pfizer Inc
Substance Name PHENYTOIN SODIUM
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Dilantin


General Information