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"43826-068-02" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43826-068-02)
(Bora Pharmaceutical Laboratories Inc.)

NDC Code43826-068-02
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43826-068-02)
Product NDC43826-068
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name Suffix(xl)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180830
Marketing Category NameANDA
Application NumberANDA210081
ManufacturerBora Pharmaceutical Laboratories 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/43826-068-02





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