Neurontin - 0071-0805-24 - (GABAPENTIN)

Alphabetical Index


Drug Information of Neurontin

Product NDC: 0071-0805
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: 0071-0805
Labeler Name: Parke-Davis Div of Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020235
Marketing Category: NDA
Start Marketing Date: 19931230

Package Information of Neurontin

Package NDC: 0071-0805-24
Package Description: 100 CAPSULE in 1 BOTTLE (0071-0805-24)

NDC Information of Neurontin

NDC Code 0071-0805-24
Proprietary Name Neurontin
Package Description 100 CAPSULE in 1 BOTTLE (0071-0805-24)
Product NDC 0071-0805
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 Parke-Davis Div of Pfizer 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