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"61919-563-72" National Drug Code (NDC)

Gabapentin 120 TABLET in 1 BOTTLE (61919-563-72)
(DIRECT RX)

NDC Code61919-563-72
Package Description120 TABLET in 1 BOTTLE (61919-563-72)
Product NDC61919-563
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20160830
Marketing Category NameANDA
Application NumberANDA202764
ManufacturerDIRECT RX
Substance NameGABAPENTIN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

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