DILANTIN - 49349-099-02 - (PHENYTOIN SODIUM)

Alphabetical Index


Drug Information of DILANTIN

Product NDC: 49349-099
Proprietary Name: DILANTIN
Non Proprietary Name: PHENYTOIN SODIUM
Active Ingredient(s): 30    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: 49349-099
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084349
Marketing Category: ANDA
Start Marketing Date: 20101130

Package Information of DILANTIN

Package NDC: 49349-099-02
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (49349-099-02)

NDC Information of DILANTIN

NDC Code 49349-099-02
Proprietary Name DILANTIN
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (49349-099-02)
Product NDC 49349-099
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PHENYTOIN SODIUM
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101130
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name PHENYTOIN SODIUM
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of DILANTIN


General Information