"16729-444-16" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-444-16)
(Accord Healthcare Inc.)

NDC Code16729-444-16
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-444-16)
Product NDC16729-444
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20190325
Marketing Category NameANDA
Application NumberANDA210497
ManufacturerAccord Healthcare Inc.
Substance NameBUPROPION HYDROCHLORIDE
Strength300
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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