Gabapentin - 65862-524-31 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 65862-524
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 800    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 65862-524
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200651
Marketing Category: ANDA
Start Marketing Date: 20111006

Package Information of Gabapentin

Package NDC: 65862-524-31
Package Description: 1700 TABLET, FILM COATED in 1 BOTTLE (65862-524-31)

NDC Information of Gabapentin

NDC Code 65862-524-31
Proprietary Name Gabapentin
Package Description 1700 TABLET, FILM COATED in 1 BOTTLE (65862-524-31)
Product NDC 65862-524
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111006
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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