"50228-523-90" National Drug Code (NDC)

Gabapentin 90 TABLET in 1 BOTTLE (50228-523-90)
(ScieGen Pharmaceuticals, Inc.)

NDC Code50228-523-90
Package Description90 TABLET in 1 BOTTLE (50228-523-90)
Product NDC50228-523
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20250920
Marketing Category NameANDA
Application NumberANDA218491
ManufacturerScieGen Pharmaceuticals, Inc.
Substance NameGABAPENTIN
Strength300
Strength Unitmg/1
Pharmacy ClassesDecreased Central Nervous System Disorganized Electrical Activity [PE]

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