Gabapentin - 50383-311-09 - (Gabapentin)

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Drug Information of Gabapentin

Product NDC: 50383-311
Proprietary Name: Gabapentin
Non Proprietary Name: Gabapentin
Active Ingredient(s): 250    mg/5mL & nbsp;   Gabapentin
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Gabapentin

Product NDC: 50383-311
Labeler Name: Hi-Tech Pharmacal Co., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078974
Marketing Category: ANDA
Start Marketing Date: 20110223

Package Information of Gabapentin

Package NDC: 50383-311-09
Package Description: 4 TRAY in 1 CASE (50383-311-09) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-311-06) > 6 mL in 1 CUP, UNIT-DOSE

NDC Information of Gabapentin

NDC Code 50383-311-09
Proprietary Name Gabapentin
Package Description 4 TRAY in 1 CASE (50383-311-09) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-311-06) > 6 mL in 1 CUP, UNIT-DOSE
Product NDC 50383-311
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gabapentin
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20110223
Marketing Category Name ANDA
Labeler Name Hi-Tech Pharmacal Co., Inc.
Substance Name GABAPENTIN
Strength Number 250
Strength Unit mg/5mL
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Gabapentin


General Information