Gabapentin - 52959-789-30 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 52959-789
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: 52959-789
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077662
Marketing Category: ANDA
Start Marketing Date: 20060401

Package Information of Gabapentin

Package NDC: 52959-789-30
Package Description: 30 TABLET in 1 BOTTLE (52959-789-30)

NDC Information of Gabapentin

NDC Code 52959-789-30
Proprietary Name Gabapentin
Package Description 30 TABLET in 1 BOTTLE (52959-789-30)
Product NDC 52959-789
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060401
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
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