"63304-724-90" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-724-90)
(Sun Pharmaceutical Industries, Inc.)

NDC Code63304-724-90
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-724-90)
Product NDC63304-724
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20210101
Marketing Category NameANDA
Application NumberANDA203650
ManufacturerSun Pharmaceutical Industries, 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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