ZYBAN is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Glaxosmithkline Llc. The primary component is Bupropion Hydrochloride.
| Product ID | 0173-0556_72435712-b707-4d63-a9a4-697a3bfa2bc6 |
| NDC | 0173-0556 |
| Product Type | Human Prescription Drug |
| Proprietary Name | ZYBAN |
| Generic Name | Bupropion Hydrochloride |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 1997-05-28 |
| Marketing Category | NDA / NDA |
| Application Number | NDA020711 |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | BUPROPION HYDROCHLORIDE |
| Active Ingredient Strength | 150 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 | 2020-12-31 |
| Marketing Start Date | 1997-05-28 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA020711 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-05-28 |
| Marketing End Date | 2016-07-31 |
| Marketing Category | NDA |
| Application Number | NDA020711 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-05-28 |
| Marketing End Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| BUPROPION HYDROCHLORIDE | 150 mg/1 |
| SPL SET ID: | a3327c31-d987-40ec-b3b5-097bbf2f4f8c |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0173-0556 | ZYBAN | bupropion hydrochloride |
| 0115-5445 | Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE |
| 0115-6811 | Bupropion Hydrochloride | BUPROPION HYDROCHLORIDE |
| 0185-0410 | Bupropion Hydrochloride | Bupropion Hydrochloride |
| 0185-0415 | Bupropion Hydrochloride | Bupropion Hydrochloride |
| 0185-1111 | Bupropion Hydrochloride | Bupropion Hydrochloride |
| 0173-0135 | WELLBUTRIN | bupropion hydrochloride |
| 0173-0722 | WELLBUTRIN | bupropion hydrochloride |
| 0173-0947 | WELLBUTRIN | bupropion hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ZYBAN 75244077 2172529 Dead/Cancelled |
GLAXO GROUP LIMITED 1997-02-19 |
![]() ZYBAN 75165464 2144141 Live/Registered |
GLAXO GROUP LIMITED 1996-09-13 |
![]() ZYBAN 72362385 0919655 Live/Registered |
MALLINCKRODT CHEMICAL WORKS 1970-06-11 |