NDC Code | 21695-578-30 |
Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (21695-578-30) |
Product NDC | 21695-578 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Bupropion Hydrochloride |
Proprietary Name Suffix | Xl |
Non-Proprietary Name | Bupropion Hydrochloride |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20070613 |
Marketing Category Name | ANDA |
Application Number | ANDA077715 |
Manufacturer | Rebel Distributors Corp |
Substance Name | BUPROPION HYDROCHLORIDE |
Strength | 300 |
Strength Unit | mg/1 |
Pharmacy Classes | Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |