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"70010-785-05" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-785-05)
(Granules Pharmaceuticals Inc.)

NDC Code70010-785-05
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-785-05)
Product NDC70010-785
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20221215
Marketing Category NameANDA
Application NumberANDA215568
ManufacturerGranules 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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70010-785-05





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