bupropion Hydrochloride
- Product NDC
- 71335-2875
- 11-digit product format
- 713352875
- Labeler code
- 71335
- Product ID
- 71335-2875_cd607962-0181-41ca-89a1-b719ef13656b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206975
- Marketing category
- ANDA
- Marketing start
- 2016-08-19
- 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
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 71335-2875-1 | 71335287501 | 100 TABLET in 1 BOTTLE (71335-2875-1) | 100 tablet | 2025-10-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| bupropion Hydrochloride | Bryant Ranch Prepack | 2025-10-22 | HUMAN PRESCRIPTION DRUG LABEL | 100 |