Gabapentin - 68788-9923-1 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 68788-9923
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 600    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 68788-9923
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200651
Marketing Category: ANDA
Start Marketing Date: 20120127

Package Information of Gabapentin

Package NDC: 68788-9923-1
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (68788-9923-1)

NDC Information of Gabapentin

NDC Code 68788-9923-1
Proprietary Name Gabapentin
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (68788-9923-1)
Product NDC 68788-9923
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120127
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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