Gabapentin - 49349-265-02 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 49349-265
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 400    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 49349-265
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078428
Marketing Category: ANDA
Start Marketing Date: 20110331

Package Information of Gabapentin

Package NDC: 49349-265-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (49349-265-02)

NDC Information of Gabapentin

NDC Code 49349-265-02
Proprietary Name Gabapentin
Package Description 30 CAPSULE in 1 BLISTER PACK (49349-265-02)
Product NDC 49349-265
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110331
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name GABAPENTIN
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information