Gabapentin - 55154-2077-0 - (Gabapentin)

Alphabetical Index


Drug Information of Gabapentin

Product NDC: 55154-2077
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 600    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 55154-2077
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077662
Marketing Category: ANDA
Start Marketing Date: 20070802

Package Information of Gabapentin

Package NDC: 55154-2077-0
Package Description: 1 BLISTER PACK in 1 BAG (55154-2077-0) > 10 TABLET in 1 BLISTER PACK

NDC Information of Gabapentin

NDC Code 55154-2077-0
Proprietary Name Gabapentin
Package Description 1 BLISTER PACK in 1 BAG (55154-2077-0) > 10 TABLET in 1 BLISTER PACK
Product NDC 55154-2077
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070802
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name GABAPENTIN
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information