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"16571-862-10" National Drug Code (NDC)

Bupropion Hydrochloride 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-862-10)
(Rising Pharma Holdings, Inc.)

NDC Code16571-862-10
Package Description1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-862-10)
Product NDC16571-862
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20220801
Marketing Category NameANDA
Application NumberANDA211020
ManufacturerRising Pharma Holdings, 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/16571-862-10





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