Gabapentin - 0904-5631-40 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 0904-5631
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: 0904-5631
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075360
Marketing Category: ANDA
Start Marketing Date: 20050406

Package Information of Gabapentin

Package NDC: 0904-5631-40
Package Description: 500 CAPSULE in 1 BOTTLE (0904-5631-40)

NDC Information of Gabapentin

NDC Code 0904-5631-40
Proprietary Name Gabapentin
Package Description 500 CAPSULE in 1 BOTTLE (0904-5631-40)
Product NDC 0904-5631
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050406
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
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