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"68382-353-05" National Drug Code (NDC)

Bupropion 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-353-05)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-353-05
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-353-05)
Product NDC68382-353
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion
Non-Proprietary NameBupropion
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180802
Marketing Category NameANDA
Application NumberANDA201567
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameBUPROPION HYDROCHLORIDE
Strength150
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/68382-353-05





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