bupropion Hydrochloride
- Product NDC
- 70934-704
- 11-digit product format
- 709340704
- Labeler code
- 70934
- Product ID
- 70934-704_aa5407f2-3c67-528d-e053-2a95a90a8975
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA206975
- Marketing category
- ANDA
- Marketing start
- 2020-05-13
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| ZG7E5POY8O | BUPROPION HYDROCHLORIDE | 31677-93-7 | BUPROPION HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-704-60 | 70934070460 | 60 TABLET in 1 BOTTLE, PLASTIC (70934-704-60) | 60 tablet | 2020-05-13 | 0000-00-00 | No | No | Current |
| 70934-704-90 | 70934070490 | 90 TABLET in 1 BOTTLE, PLASTIC (70934-704-90) | 90 tablet | 2020-05-29 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| bupropion Hydrochloride | Denton Pharma, Inc. dba Northwind Pharmaceuticals | 2020-07-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |