Gabapentin - 68084-123-01 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 68084-123
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: 68084-123
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077662
Marketing Category: ANDA
Start Marketing Date: 20070813

Package Information of Gabapentin

Package NDC: 68084-123-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-123-01) > 10 TABLET in 1 BLISTER PACK (68084-123-11)

NDC Information of Gabapentin

NDC Code 68084-123-01
Proprietary Name Gabapentin
Package Description 10 BLISTER PACK in 1 CARTON (68084-123-01) > 10 TABLET in 1 BLISTER PACK (68084-123-11)
Product NDC 68084-123
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070813
Marketing Category Name ANDA
Labeler Name American Health Packaging
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