Gabapentin - 50436-7286-1 - (Gabapentin)

Alphabetical Index


Drug Information of Gabapentin

Product NDC: 50436-7286
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: 50436-7286
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076017
Marketing Category: ANDA
Start Marketing Date: 20110421

Package Information of Gabapentin

Package NDC: 50436-7286-1
Package Description: 30 TABLET in 1 BOTTLE (50436-7286-1)

NDC Information of Gabapentin

NDC Code 50436-7286-1
Proprietary Name Gabapentin
Package Description 30 TABLET in 1 BOTTLE (50436-7286-1)
Product NDC 50436-7286
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110421
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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