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Phenytoin Infatabs - 59762-5210-1 - (PHENYTOIN)

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Drug Information of Phenytoin Infatabs

Product NDC: 59762-5210
Proprietary Name: Phenytoin Infatabs
Non Proprietary Name: PHENYTOIN
Active Ingredient(s): 50    mg/1 & nbsp;   PHENYTOIN
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Phenytoin Infatabs

Product NDC: 59762-5210
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084427
Marketing Category: ANDA
Start Marketing Date: 20121227

Package Information of Phenytoin Infatabs

Package NDC: 59762-5210-1
Package Description: 100 TABLET, CHEWABLE in 1 BOTTLE (59762-5210-1)

NDC Information of Phenytoin Infatabs

NDC Code 59762-5210-1
Proprietary Name Phenytoin Infatabs
Package Description 100 TABLET, CHEWABLE in 1 BOTTLE (59762-5210-1)
Product NDC 59762-5210
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PHENYTOIN
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20121227
Marketing Category Name ANDA
Labeler Name Greenstone LLC
Substance Name PHENYTOIN
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Phenytoin Infatabs


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