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"70377-034-13" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70377-034-13)
(Biocon Pharma Inc.,)

NDC Code70377-034-13
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70377-034-13)
Product NDC70377-034
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20190128
Marketing Category NameANDA
Application NumberANDA211020
ManufacturerBiocon Pharma 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/70377-034-13





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