"80425-0468-1" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0468-1)
(Advanced Rx of Tennessee, LLC)

NDC Code80425-0468-1
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0468-1)
Product NDC80425-0468
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20250101
Marketing Category NameANDA
Application NumberANDA207224
ManufacturerAdvanced Rx of Tennessee, LLC
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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