"72189-619-72" National Drug Code (NDC)

Gabapentin 120 TABLET in 1 BOTTLE (72189-619-72)
(Direct_Rx)

NDC Code72189-619-72
Package Description120 TABLET in 1 BOTTLE (72189-619-72)
Product NDC72189-619
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20250318
Marketing Category NameANDA
Application NumberANDA206402
ManufacturerDirect_Rx
Substance NameGABAPENTIN
Strength800
Strength Unitmg/1
Pharmacy ClassesDecreased Central Nervous System Disorganized Electrical Activity [PE]

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