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"67046-699-30" National Drug Code (NDC)

Bupropion 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-699-30)
(Coupler Enterprises Inc)

NDC Code67046-699-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-699-30)
Product NDC67046-699
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion
Proprietary Name SuffixXl
Non-Proprietary NameBupropion
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20170214
Marketing Category NameANDA
Application NumberANDA090693
ManufacturerCoupler Enterprises 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/67046-699-30





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