NDC Code | 72789-070-90 |
Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-90) |
Product NDC | 72789-070 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Bupropion Hydrochloride |
Non-Proprietary Name | Bupropion Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20060117 |
Marketing Category Name | ANDA |
Application Number | ANDA076143 |
Manufacturer | PD-Rx Pharmaceuticals, Inc. |
Substance Name | BUPROPION HYDROCHLORIDE |
Strength | 100 |
Strength Unit | mg/1 |
Pharmacy Classes | Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA] |