Gabapentin - 55289-959-90 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 55289-959
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: 55289-959
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077662
Marketing Category: ANDA
Start Marketing Date: 20060401

Package Information of Gabapentin

Package NDC: 55289-959-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (55289-959-90)

NDC Information of Gabapentin

NDC Code 55289-959-90
Proprietary Name Gabapentin
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (55289-959-90)
Product NDC 55289-959
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 PD-Rx Pharmaceuticals, 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