"52125-984-19" National Drug Code (NDC)

Gabapentin 90 TABLET in 1 BOTTLE (52125-984-19)
(REMEDYREPACK INC.)

NDC Code52125-984-19
Package Description90 TABLET in 1 BOTTLE (52125-984-19)
Product NDC52125-984
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20160408
End Marketing Date20170526
Marketing Category NameANDA
Application NumberANDA202764
ManufacturerREMEDYREPACK INC.
Substance NameGABAPENTIN
Strength800
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

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