Gabapentin - 49349-533-20 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 49349-533
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 800    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 49349-533
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077525
Marketing Category: ANDA
Start Marketing Date: 20110923

Package Information of Gabapentin

Package NDC: 49349-533-20
Package Description: 100 TABLET in 1 CANISTER (49349-533-20)

NDC Information of Gabapentin

NDC Code 49349-533-20
Proprietary Name Gabapentin
Package Description 100 TABLET in 1 CANISTER (49349-533-20)
Product NDC 49349-533
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110923
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name GABAPENTIN
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information