Gabapentin - 35356-709-00 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 35356-709
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 100    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 35356-709
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090705
Marketing Category: ANDA
Start Marketing Date: 20100517

Package Information of Gabapentin

Package NDC: 35356-709-00
Package Description: 90 CAPSULE in 1 BOTTLE (35356-709-00)

NDC Information of Gabapentin

NDC Code 35356-709-00
Proprietary Name Gabapentin
Package Description 90 CAPSULE in 1 BOTTLE (35356-709-00)
Product NDC 35356-709
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100517
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name GABAPENTIN
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information