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Phenytoin Sodium - 76237-226-30 - (phenytoin sodium)

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Drug Information of Phenytoin Sodium

Product NDC: 76237-226
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: 76237-226
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040298
Marketing Category: ANDA
Start Marketing Date: 20110919

Package Information of Phenytoin Sodium

Package NDC: 76237-226-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-226-30) > 5 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Phenytoin Sodium

NDC Code 76237-226-30
Proprietary Name Phenytoin Sodium
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-226-30) > 5 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 76237-226
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name phenytoin sodium
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110919
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
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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