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"69097-879-12" National Drug Code (NDC)

Bupropion Hydrochloride (sr) 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-879-12)
(Cipla USA Inc.,)

NDC Code69097-879-12
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-879-12)
Product NDC69097-879
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride (sr)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20160725
Marketing Category NameANDA
Application NumberANDA206674
ManufacturerCipla USA Inc.,
Substance NameBUPROPION HYDROCHLORIDE
Strength200
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/69097-879-12





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