"69844-064-04" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET in 1 BOTTLE (69844-064-04)
(Graviti Pharmaceuticals Private Limited)

NDC Code69844-064-04
Package Description500 TABLET in 1 BOTTLE (69844-064-04)
Product NDC69844-064
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameExtended-release
Dosage FormTABLET
UsageORAL
Start Marketing Date20190128
Marketing Category NameANDA
Application NumberANDA211020
ManufacturerGraviti Pharmaceuticals Private Limited
Substance NameBUPROPION HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesAminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]

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