Gabapentin - 21695-056-42 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 21695-056
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 300    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 21695-056
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075360
Marketing Category: ANDA
Start Marketing Date: 20060829

Package Information of Gabapentin

Package NDC: 21695-056-42
Package Description: 42 CAPSULE in 1 BOTTLE (21695-056-42)

NDC Information of Gabapentin

NDC Code 21695-056-42
Proprietary Name Gabapentin
Package Description 42 CAPSULE in 1 BOTTLE (21695-056-42)
Product NDC 21695-056
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20060829
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name GABAPENTIN
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information