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"69097-875-12" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-875-12)
(CIPLA USA INC.,)

NDC Code69097-875-12
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-875-12)
Product NDC69097-875
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name Suffix(xl)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20160829
Marketing Category NameANDA
Application NumberANDA206556
ManufacturerCIPLA 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/69097-875-12





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