Gabapentin - 67877-224-01 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 67877-224
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: 67877-224
Labeler Name: Ascend Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090858
Marketing Category: ANDA
Start Marketing Date: 20110129

Package Information of Gabapentin

Package NDC: 67877-224-01
Package Description: 100 CAPSULE in 1 BOTTLE (67877-224-01)

NDC Information of Gabapentin

NDC Code 67877-224-01
Proprietary Name Gabapentin
Package Description 100 CAPSULE in 1 BOTTLE (67877-224-01)
Product NDC 67877-224
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110129
Marketing Category Name ANDA
Labeler Name Ascend Laboratories, LLC
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