Aplenzin is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Bausch Health Us, Llc. The primary component is Bupropion Hydrobromide.
Product ID | 0187-5812_23b09d2e-0c63-4d09-9612-ed7efd542729 |
NDC | 0187-5812 |
Product Type | Human Prescription Drug |
Proprietary Name | Aplenzin |
Generic Name | Bupropion Hydrobromide |
Dosage Form | Tablet, Extended Release |
Route of Administration | ORAL |
Marketing Start Date | 2008-04-23 |
Marketing Category | NDA / NDA |
Application Number | NDA022108 |
Labeler Name | Bausch Health US, LLC |
Substance Name | BUPROPION HYDROBROMIDE |
Active Ingredient Strength | 522 mg/1 |
Pharm Classes | Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2008-04-23 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA022108 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-04-23 |
Marketing Category | NDA |
Application Number | NDA022108 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2008-04-23 |
Ingredient | Strength |
---|---|
BUPROPION HYDROBROMIDE | 522 mg/1 |
SPL SET ID: | 6494d2d9-0ce4-4126-b1c7-49684395942b |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0187-5810 | Aplenzin | bupropion hydrobromide |
0187-5811 | Aplenzin | bupropion hydrobromide |
0187-5812 | Aplenzin | bupropion hydrobromide |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
APLENZIN 78340327 not registered Dead/Abandoned |
Biovail Laboratories International SRL 2003-12-12 |
APLENZIN 77594316 3650117 Live/Registered |
BAUSCH HEALTH IRELAND LIMITED 2008-10-16 |