| NDC Code: |
52125-508 |
| Proprietary Name: |
Bupropion HydrochlorideXL |
| Suffix: |
XL |
| Non-Proprietary Name: |
Bupropion Hydrochloride |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
03-06-2013 |
| Category Name: |
ANDA |
| Application Number: |
ANDA077715 |
| Labeler: |
REMEDYREPACK INC. |
| Substance Name: |
BUPROPION HYDROCHLORIDE |
| Active Numerator Strength: |
300 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |
| DEA Schedule: |
|
