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"61919-350-72" National Drug Code (NDC)

Gabapentin 120 TABLET in 1 BOTTLE (61919-350-72)
(Direct_Rx)

NDC Code61919-350-72
Package Description120 TABLET in 1 BOTTLE (61919-350-72)
Product NDC61919-350
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20190808
Marketing Category NameANDA
Application NumberANDA077662
ManufacturerDirect_Rx
Substance NameGABAPENTIN
Strength800
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-350-72





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