Gabapentin - 68084-079-01 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 68084-079
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 100    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 68084-079
Labeler Name: AMERISOURCEBERGEN DRUG CORPORATION
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075350
Marketing Category: ANDA
Start Marketing Date: 20041210

Package Information of Gabapentin

Package NDC: 68084-079-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-079-01) > 10 CAPSULE in 1 BLISTER PACK (68084-079-11)

NDC Information of Gabapentin

NDC Code 68084-079-01
Proprietary Name Gabapentin
Package Description 10 BLISTER PACK in 1 CARTON (68084-079-01) > 10 CAPSULE in 1 BLISTER PACK (68084-079-11)
Product NDC 68084-079
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20041210
Marketing Category Name ANDA
Labeler Name AMERISOURCEBERGEN DRUG CORPORATION
Substance Name GABAPENTIN
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information