NDC Code | 68788-7807-9 |
Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7807-9) |
Product NDC | 68788-7807 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Bupropion Hydrochloride |
Proprietary Name Suffix | Sr |
Non-Proprietary Name | Bupropion Hydrochloride |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20201028 |
Marketing Category Name | ANDA |
Application Number | ANDA205794 |
Manufacturer | Preferred Pharmaceuticals, Inc. |
Substance Name | BUPROPION HYDROCHLORIDE |
Strength | 150 |
Strength Unit | mg/1 |
Pharmacy Classes | Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA] |