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"70436-059-02" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-02)
(Slate Run Pharmaceuticals, LLC)

NDC Code70436-059-02
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-02)
Product NDC70436-059
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixSr
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20201102
Marketing Category NameANDA
Application NumberANDA211347
ManufacturerSlate Run Pharmaceuticals, LLC
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/70436-059-02





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