Gabapentin - 42549-512-02 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 42549-512
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: 42549-512
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078428
Marketing Category: ANDA
Start Marketing Date: 20091124

Package Information of Gabapentin

Package NDC: 42549-512-02
Package Description: 112 CAPSULE in 1 BOTTLE (42549-512-02)

NDC Information of Gabapentin

NDC Code 42549-512-02
Proprietary Name Gabapentin
Package Description 112 CAPSULE in 1 BOTTLE (42549-512-02)
Product NDC 42549-512
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20091124
Marketing Category Name ANDA
Labeler Name STAT Rx USA 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