Gabapentin - 54868-5195-4 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 54868-5195
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 800    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 54868-5195
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077662
Marketing Category: ANDA
Start Marketing Date: 20041216

Package Information of Gabapentin

Package NDC: 54868-5195-4
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (54868-5195-4)

NDC Information of Gabapentin

NDC Code 54868-5195-4
Proprietary Name Gabapentin
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (54868-5195-4)
Product NDC 54868-5195
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041216
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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