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"71209-052-11" National Drug Code (NDC)

Bupropion Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (71209-052-11)
(Cadila Pharmaceuticals Limited)

NDC Code71209-052-11
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (71209-052-11)
Product NDC71209-052
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200116
Marketing Category NameANDA
Application NumberANDA208606
ManufacturerCadila Pharmaceuticals Limited
Substance NameBUPROPION HYDROCHLORIDE
Strength75
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/71209-052-11





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