Gabapentin - 16714-661-02 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 16714-661
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 100    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 16714-661
Labeler Name: NorthStar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078787
Marketing Category: ANDA
Start Marketing Date: 20080131

Package Information of Gabapentin

Package NDC: 16714-661-02
Package Description: 500 CAPSULE in 1 BOTTLE (16714-661-02)

NDC Information of Gabapentin

NDC Code 16714-661-02
Proprietary Name Gabapentin
Package Description 500 CAPSULE in 1 BOTTLE (16714-661-02)
Product NDC 16714-661
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080131
Marketing Category Name ANDA
Labeler Name NorthStar Rx LLC
Substance Name GABAPENTIN
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information