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"69367-288-05" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-288-05)
(Westminster Pharmaceuticals, LLC)

NDC Code69367-288-05
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-288-05)
Product NDC69367-288
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20171001
Marketing Category NameANDA
Application NumberANDA207224
ManufacturerWestminster 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/69367-288-05





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