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"47335-954-13" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-13)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-954-13
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-13)
Product NDC47335-954
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20141225
Marketing Category NameANDA
Application NumberANDA200695
ManufacturerSun Pharmaceutical Industries, 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/47335-954-13





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