Gabapentin - 52343-030-01 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 52343-030
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: 52343-030
Labeler Name: Gen-Source Rx
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078787
Marketing Category: ANDA
Start Marketing Date: 20080131

Package Information of Gabapentin

Package NDC: 52343-030-01
Package Description: 100 CAPSULE in 1 BOTTLE (52343-030-01)

NDC Information of Gabapentin

NDC Code 52343-030-01
Proprietary Name Gabapentin
Package Description 100 CAPSULE in 1 BOTTLE (52343-030-01)
Product NDC 52343-030
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080131
Marketing Category Name ANDA
Labeler Name Gen-Source Rx
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