Neurontin - 52125-077-02 - (gabapentin)

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Drug Information of Neurontin

Product NDC: 52125-077
Proprietary Name: Neurontin
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 Neurontin

Product NDC: 52125-077
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020235
Marketing Category: NDA
Start Marketing Date: 20120917

Package Information of Neurontin

Package NDC: 52125-077-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (52125-077-02)

NDC Information of Neurontin

NDC Code 52125-077-02
Proprietary Name Neurontin
Package Description 30 CAPSULE in 1 BLISTER PACK (52125-077-02)
Product NDC 52125-077
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120917
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
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 Neurontin


General Information