GABAPENTIN - 62756-138-04 - (GABAPENTIN)

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Drug Information of GABAPENTIN

Product NDC: 62756-138
Proprietary Name: GABAPENTIN
Non Proprietary Name: GABAPENTIN
Active Ingredient(s): 300    mg/1 & nbsp;   GABAPENTIN
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of GABAPENTIN

Product NDC: 62756-138
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077242
Marketing Category: ANDA
Start Marketing Date: 20060824

Package Information of GABAPENTIN

Package NDC: 62756-138-04
Package Description: 1000 CAPSULE in 1 BOTTLE (62756-138-04)

NDC Information of GABAPENTIN

NDC Code 62756-138-04
Proprietary Name GABAPENTIN
Package Description 1000 CAPSULE in 1 BOTTLE (62756-138-04)
Product NDC 62756-138
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GABAPENTIN
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20060824
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name GABAPENTIN
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of GABAPENTIN


General Information