Bupropion Hydrochloride
- Product NDC
- 50436-9101
- 11-digit product format
- 504369101
- Labeler code
- 50436
- Product ID
- 50436-9101_ebfed222-df25-4474-873c-aea5e9076b43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA075584
- Marketing category
- ANDA
- Marketing start
- 2000-02-07
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 100 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 50436-9101-2 | Bupropion Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 4 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| BUPROPION HYDROCHLORIDE | ACTIVE INGREDIENT | ZG7E5POY8O | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | |
| BUPROPION | ACTIVE MOIETY | 01ZG3TPX31 | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | |
| HYPROMELLOSE 2910 (15 MPA.S) | INACTIVE INGREDIENT | 36SFW2JZ0W | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | |
| POTASSIUM CHLORIDE | INACTIVE INGREDIENT | 660YQ98I10 | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | |
| TRIETHYL CITRATE | INACTIVE INGREDIENT | 8Z96QXD6UM | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-9101 | BUPROPION HYDROCHLORIDE TABLET, FILM COATED [UNIT DOSE SERVICES] | 4 | Legacy NDC, 1 package rows | 20170702_92f0c82c-8b9b-4bad-9de2-6e1b81588000.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-9101-2 | 50436910102 | 60 in 1 BOTTLE | Historical |