Gabapentin - 54868-5219-1 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 54868-5219
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 600    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 54868-5219
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077662
Marketing Category: ANDA
Start Marketing Date: 20050214

Package Information of Gabapentin

Package NDC: 54868-5219-1
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (54868-5219-1)

NDC Information of Gabapentin

NDC Code 54868-5219-1
Proprietary Name Gabapentin
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (54868-5219-1)
Product NDC 54868-5219
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050214
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name GABAPENTIN
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information