Gabapentin - 49349-928-20 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 49349-928
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: 49349-928
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090705
Marketing Category: ANDA
Start Marketing Date: 20120323

Package Information of Gabapentin

Package NDC: 49349-928-20
Package Description: 100 CAPSULE in 1 VIAL (49349-928-20)

NDC Information of Gabapentin

NDC Code 49349-928-20
Proprietary Name Gabapentin
Package Description 100 CAPSULE in 1 VIAL (49349-928-20)
Product NDC 49349-928
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120323
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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