"61919-843-90" National Drug Code (NDC)

Gabapentin 90 TABLET in 1 BOTTLE (61919-843-90)
(DirectRX)

NDC Code61919-843-90
Package Description90 TABLET in 1 BOTTLE (61919-843-90)
Product NDC61919-843
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20151125
Marketing Category NameANDA
Application NumberANDA202764
ManufacturerDirectRX
Substance NameGABAPENTIN
Strength800
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

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