NDC Code |
0378-5521-05 |
Proprietary Name |
Bupropion Hydrochloride |
Package Description |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-5521-05) |
Product NDC |
0378-5521 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Bupropion Hydrochloride |
Dosage Form Name |
TABLET, FILM COATED, EXTENDED RELEASE |
Route Name |
ORAL |
Start Marketing Date |
20120703 |
Marketing Category Name |
ANDA |
Labeler Name |
Mylan Pharmaceuticals Inc. |
Substance Name |
BUPROPION HYDROCHLORIDE |
Strength Number |
150 |
Strength Unit |
mg/1 |
Pharmaceutical Classes |
Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |