GABAPENTIN - 21695-059-60 - (GABAPENTIN)

Alphabetical Index


Drug Information of GABAPENTIN

Product NDC: 21695-059
Proprietary Name: GABAPENTIN
Non Proprietary Name: GABAPENTIN
Active Ingredient(s): 800    mg/1 & nbsp;   GABAPENTIN
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of GABAPENTIN

Product NDC: 21695-059
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077525
Marketing Category: ANDA
Start Marketing Date: 20060824

Package Information of GABAPENTIN

Package NDC: 21695-059-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (21695-059-60)

NDC Information of GABAPENTIN

NDC Code 21695-059-60
Proprietary Name GABAPENTIN
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (21695-059-60)
Product NDC 21695-059
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GABAPENTIN
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060824
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name GABAPENTIN
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of GABAPENTIN


General Information