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Extended Phenytoin Sodium - 52125-176-02 - (PHENYTOIN SODIUM)

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Drug Information of Extended Phenytoin Sodium

Product NDC: 52125-176
Proprietary Name: Extended Phenytoin Sodium
Non Proprietary Name: PHENYTOIN SODIUM
Active Ingredient(s): 100    mg/1 & nbsp;   PHENYTOIN SODIUM
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Extended Phenytoin Sodium

Product NDC: 52125-176
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040765
Marketing Category: ANDA
Start Marketing Date: 20121226

Package Information of Extended Phenytoin Sodium

Package NDC: 52125-176-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (52125-176-02)

NDC Information of Extended Phenytoin Sodium

NDC Code 52125-176-02
Proprietary Name Extended Phenytoin Sodium
Package Description 30 CAPSULE in 1 BLISTER PACK (52125-176-02)
Product NDC 52125-176
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PHENYTOIN SODIUM
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20121226
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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 Extended Phenytoin Sodium


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