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"63739-132-33" National Drug Code (NDC)

Bupropion Hydrochloride 3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-132-33) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(McKesson Corporation DBA SKY Packaging)

NDC Code63739-132-33
Package Description3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-132-33) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC63739-132
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name Suffix(xl)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20230912
Marketing Category NameANDA
Application NumberANDA210081
ManufacturerMcKesson Corporation DBA SKY Packaging
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63739-132-33





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