"50228-176-30" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-30)
(ScieGen Pharmaceuticals, Inc.)

NDC Code50228-176-30
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-30)
Product NDC50228-176
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixSr
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180420
Marketing Category NameANDA
Application NumberANDA205794
ManufacturerScieGen Pharmaceuticals, Inc.
Substance NameBUPROPION HYDROCHLORIDE
Strength200
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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