"55700-849-30" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-849-30)
(Quality Care Products, LLC)

NDC Code55700-849-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-849-30)
Product NDC55700-849
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20200316
Marketing Category NameANDA
Application NumberANDA210497
ManufacturerQuality Care Products, LLC
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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