"21695-295-60" National Drug Code (NDC)

Bupropion Hydrochloride 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-295-60)
(Rebel Distributors Corp.)

NDC Code21695-295-60
Package Description60 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-295-60)
Product NDC21695-295
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20090901
Marketing Category NameANDA
Application NumberANDA079095
ManufacturerRebel Distributors Corp.
Substance NameBUPROPION HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]

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