Gabapentin - 49999-784-90 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 49999-784
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 600    mg/1 & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 49999-784
Labeler Name: Lake Erie Medica & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077662
Marketing Category: ANDA
Start Marketing Date: 20111104

Package Information of Gabapentin

Package NDC: 49999-784-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (49999-784-90)

NDC Information of Gabapentin

NDC Code 49999-784-90
Proprietary Name Gabapentin
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (49999-784-90)
Product NDC 49999-784
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111104
Marketing Category Name ANDA
Labeler Name Lake Erie Medica & Surgical Supply DBA Quality Care Products LLC
Substance Name GABAPENTIN
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information