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Extended Phenytoin Sodium - 65162-212-50 - (Phenytoin Sodium)

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Drug Information of Extended Phenytoin Sodium

Product NDC: 65162-212
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: 65162-212
Labeler Name: Amneal Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040765
Marketing Category: ANDA
Start Marketing Date: 20091216

Package Information of Extended Phenytoin Sodium

Package NDC: 65162-212-50
Package Description: 500 CAPSULE in 1 BOTTLE (65162-212-50)

NDC Information of Extended Phenytoin Sodium

NDC Code 65162-212-50
Proprietary Name Extended Phenytoin Sodium
Package Description 500 CAPSULE in 1 BOTTLE (65162-212-50)
Product NDC 65162-212
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phenytoin Sodium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20091216
Marketing Category Name ANDA
Labeler Name Amneal Pharmaceuticals, LLC
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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