PHENYTOIN - 16590-815-30 - (PHENYTOIN SODIUM)

Alphabetical Index


Drug Information of PHENYTOIN

Product NDC: 16590-815
Proprietary Name: PHENYTOIN
Non Proprietary Name: PHENYTOIN SODIUM
Active Ingredient(s): 100    mg/1 & nbsp;   PHENYTOIN SODIUM
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of PHENYTOIN

Product NDC: 16590-815
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040298
Marketing Category: ANDA
Start Marketing Date: 20091120

Package Information of PHENYTOIN

Package NDC: 16590-815-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (16590-815-30)

NDC Information of PHENYTOIN

NDC Code 16590-815-30
Proprietary Name PHENYTOIN
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (16590-815-30)
Product NDC 16590-815
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PHENYTOIN SODIUM
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20091120
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
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


General Information