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PHENYTOIN SODIUM - 62756-402-03 - (PHENYTOIN SODIUM)

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Drug Information of PHENYTOIN SODIUM

Product NDC: 62756-402
Proprietary Name: PHENYTOIN SODIUM
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 PHENYTOIN SODIUM

Product NDC: 62756-402
Labeler Name: SUN PHARMACEUTICAL INDUSTRIES LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040621
Marketing Category: ANDA
Start Marketing Date: 20061212

Package Information of PHENYTOIN SODIUM

Package NDC: 62756-402-03
Package Description: 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-402-03)

NDC Information of PHENYTOIN SODIUM

NDC Code 62756-402-03
Proprietary Name PHENYTOIN SODIUM
Package Description 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62756-402-03)
Product NDC 62756-402
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PHENYTOIN SODIUM
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20061212
Marketing Category Name ANDA
Labeler Name SUN PHARMACEUTICAL INDUSTRIES LIMITED
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 PHENYTOIN SODIUM


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