Gabapentin - 49999-539-60 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 49999-539
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 300    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 49999-539
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075350
Marketing Category: ANDA
Start Marketing Date: 20100917

Package Information of Gabapentin

Package NDC: 49999-539-60
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC (49999-539-60)

NDC Information of Gabapentin

NDC Code 49999-539-60
Proprietary Name Gabapentin
Package Description 60 CAPSULE in 1 BOTTLE, PLASTIC (49999-539-60)
Product NDC 49999-539
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100917
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name GABAPENTIN
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information