Gabapentin - 51991-339-05 - (GABAPENTIN)

Alphabetical Index


Drug Information of Gabapentin

Product NDC: 51991-339
Proprietary Name: Gabapentin
Non Proprietary Name: GABAPENTIN
Active Ingredient(s): 400    mg/1 & nbsp;   GABAPENTIN
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 51991-339
Labeler Name: Breckenridge Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090007
Marketing Category: ANDA
Start Marketing Date: 20121015

Package Information of Gabapentin

Package NDC: 51991-339-05
Package Description: 500 CAPSULE in 1 BOTTLE (51991-339-05)

NDC Information of Gabapentin

NDC Code 51991-339-05
Proprietary Name Gabapentin
Package Description 500 CAPSULE in 1 BOTTLE (51991-339-05)
Product NDC 51991-339
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GABAPENTIN
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20121015
Marketing Category Name ANDA
Labeler Name Breckenridge Pharmaceutical, Inc.
Substance Name GABAPENTIN
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information