Gabapentin - 60760-038-30 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 60760-038
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 800    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: 60760-038
Labeler Name: St Marys Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077525
Marketing Category: ANDA
Start Marketing Date: 20101203

Package Information of Gabapentin

Package NDC: 60760-038-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (60760-038-30)

NDC Information of Gabapentin

NDC Code 60760-038-30
Proprietary Name Gabapentin
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (60760-038-30)
Product NDC 60760-038
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101203
Marketing Category Name ANDA
Labeler Name St Marys Medical Park Pharmacy
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