Gabapentin - 59115-074-99 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 59115-074
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 300    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 59115-074
Labeler Name: Hikma Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078150
Marketing Category: ANDA
Start Marketing Date: 20070709

Package Information of Gabapentin

Package NDC: 59115-074-99
Package Description: 1 CAPSULE in 1 DRUM (59115-074-99)

NDC Information of Gabapentin

NDC Code 59115-074-99
Proprietary Name Gabapentin
Package Description 1 CAPSULE in 1 DRUM (59115-074-99)
Product NDC 59115-074
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070709
Marketing Category Name ANDA
Labeler Name Hikma Pharmaceutical
Substance Name GABAPENTIN
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information