Gabapentin - 0143-9994-01 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 0143-9994
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: 0143-9994
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078150
Marketing Category: ANDA
Start Marketing Date: 20070709

Package Information of Gabapentin

Package NDC: 0143-9994-01
Package Description: 100 CAPSULE in 1 BOTTLE (0143-9994-01)

NDC Information of Gabapentin

NDC Code 0143-9994-01
Proprietary Name Gabapentin
Package Description 100 CAPSULE in 1 BOTTLE (0143-9994-01)
Product NDC 0143-9994
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070709
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
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