Gabapentin - 0093-4444-93 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 0093-4444
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 800    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 0093-4444
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076017
Marketing Category: ANDA
Start Marketing Date: 20080801

Package Information of Gabapentin

Package NDC: 0093-4444-93
Package Description: 100 BLISTER PACK in 1 BOX (0093-4444-93) > 1 TABLET in 1 BLISTER PACK (0093-4444-19)

NDC Information of Gabapentin

NDC Code 0093-4444-93
Proprietary Name Gabapentin
Package Description 100 BLISTER PACK in 1 BOX (0093-4444-93) > 1 TABLET in 1 BLISTER PACK (0093-4444-19)
Product NDC 0093-4444
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080801
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name GABAPENTIN
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information