WELLBUTRIN
- Product NDC
- 0173-0135
- 11-digit product format
- 001730135
- Labeler code
- 0173
- Product ID
- 0173-0135_5ffc8b63-7d69-4f3a-bf05-a9c138724a91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- GlaxoSmithKline LLC
- Application
- NDA020358
- Marketing category
- NDA
- Marketing start
- 1996-11-15
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- WELLBUTRIN
- Brand name suffix
- SR
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUPROPION HYDROCHLORIDE | 150 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZG7E5POY8O |
| Rxcui | 993503, 993511, 993518, 993528, 993536, 993537 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0173-0135-55 | WELLBUTRINSR | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 39 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| bupropion hydrochloride | ACTIVE INGREDIENT | ZG7E5POY8O | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| bupropion | ACTIVE MOIETY | 01ZG3TPX31 | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| CARNAUBA WAX | INACTIVE INGREDIENT | R12CBM0EIZ | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| CYSTEINE HYDROCHLORIDE | INACTIVE INGREDIENT | ZT934N0X4W | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| FD&C BLUE NO. 1 | INACTIVE INGREDIENT | H3R47K3TBD | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| POLYSORBATE 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 20 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0173-0135 | WELLBUTRIN SR (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC] | 37 | Current NDC, Legacy NDC, 1 package rows | 20250522_cbc8c074-f080-4489-a5ae-207b5fadeba3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0173-0135-55 | 00173013555 | 60 TABLET, FILM COATED in 1 BOTTLE (0173-0135-55) | 1996-11-15 | 0000-00-00 | No | No | Current |