Gabapentin - 68084-594-01 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 68084-594
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: 68084-594
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075350
Marketing Category: ANDA
Start Marketing Date: 20120305

Package Information of Gabapentin

Package NDC: 68084-594-01
Package Description: 5 BLISTER PACK in 1 CARTON (68084-594-01) > 10 CAPSULE in 1 BLISTER PACK (68084-594-11)

NDC Information of Gabapentin

NDC Code 68084-594-01
Proprietary Name Gabapentin
Package Description 5 BLISTER PACK in 1 CARTON (68084-594-01) > 10 CAPSULE in 1 BLISTER PACK (68084-594-11)
Product NDC 68084-594
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120305
Marketing Category Name ANDA
Labeler Name American Health Packaging
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