NDC Code |
52959-655-60 |
Proprietary Name |
Bupropion Hydrochloride |
Package Description |
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-655-60) |
Product NDC |
52959-655 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
bupropion hydrochloride |
Dosage Form Name |
TABLET, FILM COATED |
Route Name |
ORAL |
Start Marketing Date |
20100201 |
Marketing Category Name |
ANDA |
Labeler Name |
H.J. Harkins Company, Inc. |
Substance Name |
BUPROPION HYDROCHLORIDE |
Strength Number |
100 |
Strength Unit |
mg/1 |
Pharmaceutical Classes |
Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |