GABAPENTIN - 62756-204-03 - (GABAPENTIN)

Alphabetical Index


Drug Information of GABAPENTIN

Product NDC: 62756-204
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: 62756-204
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077525
Marketing Category: ANDA
Start Marketing Date: 20060824

Package Information of GABAPENTIN

Package NDC: 62756-204-03
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (62756-204-03)

NDC Information of GABAPENTIN

NDC Code 62756-204-03
Proprietary Name GABAPENTIN
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (62756-204-03)
Product NDC 62756-204
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 Sun Pharmaceutical Industries Limited
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