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EXTENDED PHENYTOIN SODIUM - 55289-906-60 - (EXTENDED PHENYTOIN SODIUM)

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Drug Information of EXTENDED PHENYTOIN SODIUM

Product NDC: 55289-906
Proprietary Name: EXTENDED PHENYTOIN SODIUM
Non Proprietary Name: EXTENDED PHENYTOIN SODIUM
Active Ingredient(s): 100    mg/1 & nbsp;   EXTENDED PHENYTOIN SODIUM
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of EXTENDED PHENYTOIN SODIUM

Product NDC: 55289-906
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040732
Marketing Category: ANDA
Start Marketing Date: 20080130

Package Information of EXTENDED PHENYTOIN SODIUM

Package NDC: 55289-906-60
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC (55289-906-60)

NDC Information of EXTENDED PHENYTOIN SODIUM

NDC Code 55289-906-60
Proprietary Name EXTENDED PHENYTOIN SODIUM
Package Description 60 CAPSULE in 1 BOTTLE, PLASTIC (55289-906-60)
Product NDC 55289-906
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name EXTENDED PHENYTOIN SODIUM
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080130
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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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