Neurontin - 55154-2415-0 - (gabapentin)

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Drug Information of Neurontin

Product NDC: 55154-2415
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: 55154-2415
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020235
Marketing Category: NDA
Start Marketing Date: 19931230

Package Information of Neurontin

Package NDC: 55154-2415-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-2415-0) > 1 CAPSULE in 1 BLISTER PACK

NDC Information of Neurontin

NDC Code 55154-2415-0
Proprietary Name Neurontin
Package Description 10 BLISTER PACK in 1 BAG (55154-2415-0) > 1 CAPSULE in 1 BLISTER PACK
Product NDC 55154-2415
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19931230
Marketing Category Name NDA
Labeler Name Cardinal Health
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