Gabapentin - 55154-3725-7 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 55154-3725
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: 55154-3725
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075350
Marketing Category: ANDA
Start Marketing Date: 20100123

Package Information of Gabapentin

Package NDC: 55154-3725-7
Package Description: 14 CAPSULE in 1 BLISTER PACK (55154-3725-7)

NDC Information of Gabapentin

NDC Code 55154-3725-7
Proprietary Name Gabapentin
Package Description 14 CAPSULE in 1 BLISTER PACK (55154-3725-7)
Product NDC 55154-3725
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100123
Marketing Category Name ANDA
Labeler Name Cardinal Health
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