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Phenytoin Sodium - 21695-167-30 - (Phenytoin Sodium)

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Drug Information of Phenytoin Sodium

Product NDC: 21695-167
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: 21695-167
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040684
Marketing Category: ANDA
Start Marketing Date: 20060905

Package Information of Phenytoin Sodium

Package NDC: 21695-167-30
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (21695-167-30)

NDC Information of Phenytoin Sodium

NDC Code 21695-167-30
Proprietary Name Phenytoin Sodium
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (21695-167-30)
Product NDC 21695-167
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phenytoin Sodium
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060905
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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