Gabapentin - 31722-406-05 - (Gabapentin)

Alphabetical Index


Drug Information of Gabapentin

Product NDC: 31722-406
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 800    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 31722-406
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202764
Marketing Category: ANDA
Start Marketing Date: 20121029

Package Information of Gabapentin

Package NDC: 31722-406-05
Package Description: 500 TABLET in 1 BOTTLE (31722-406-05)

NDC Information of Gabapentin

NDC Code 31722-406-05
Proprietary Name Gabapentin
Package Description 500 TABLET in 1 BOTTLE (31722-406-05)
Product NDC 31722-406
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121029
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
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