NDC Code |
49909-010-30 |
Proprietary Name |
Forfivo |
Package Description |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (49909-010-30) |
Product NDC |
49909-010 |
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 |
20121001 |
Marketing Category Name |
NDA |
Labeler Name |
Edgemont Pharmaceuticals, LLC |
Substance Name |
BUPROPION HYDROCHLORIDE |
Strength Number |
450 |
Strength Unit |
mg/1 |
Pharmaceutical Classes |
Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |