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"53002-4508-3" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-4508-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-4508-3
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-4508-3)
Product NDC53002-4508
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
ManufacturerRPK Pharmaceuticals, 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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