Gabapentin - 0615-1377-39 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 0615-1377
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: 0615-1377
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075350
Marketing Category: ANDA
Start Marketing Date: 20030912

Package Information of Gabapentin

Package NDC: 0615-1377-39
Package Description: 30 CAPSULE in 1 BLISTER PACK (0615-1377-39)

NDC Information of Gabapentin

NDC Code 0615-1377-39
Proprietary Name Gabapentin
Package Description 30 CAPSULE in 1 BLISTER PACK (0615-1377-39)
Product NDC 0615-1377
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20030912
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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