Gabapentin - 31722-221-01 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 31722-221
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: 31722-221
Labeler Name: Camber Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090705
Marketing Category: ANDA
Start Marketing Date: 20100517

Package Information of Gabapentin

Package NDC: 31722-221-01
Package Description: 24 BOTTLE in 1 CASE (31722-221-01) > 100 CAPSULE in 1 BOTTLE

NDC Information of Gabapentin

NDC Code 31722-221-01
Proprietary Name Gabapentin
Package Description 24 BOTTLE in 1 CASE (31722-221-01) > 100 CAPSULE in 1 BOTTLE
Product NDC 31722-221
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100517
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals Inc.
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