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ethosuximide - 68382-443-05 - (ethosuximide)

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Drug Information of ethosuximide

Product NDC: 68382-443
Proprietary Name: ethosuximide
Non Proprietary Name: ethosuximide
Active Ingredient(s): 250    1/1 & nbsp;   ethosuximide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of ethosuximide

Product NDC: 68382-443
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200892
Marketing Category: ANDA
Start Marketing Date: 20121010

Package Information of ethosuximide

Package NDC: 68382-443-05
Package Description: 500 CAPSULE in 1 BOTTLE (68382-443-05)

NDC Information of ethosuximide

NDC Code 68382-443-05
Proprietary Name ethosuximide
Package Description 500 CAPSULE in 1 BOTTLE (68382-443-05)
Product NDC 68382-443
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ethosuximide
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20121010
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name ETHOSUXIMIDE
Strength Number 250
Strength Unit 1/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of ethosuximide


General Information