Bupropion Hydrochloride
- Product NDC
- 71610-708
- 11-digit product format
- 716100708
- Labeler code
- 71610
- Product ID
- 71610-708_512751a6-66a2-4ce8-bb22-053853f0300b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA076143
- Marketing category
- ANDA
- Marketing start
- 2006-01-17
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 71610-708-80 | 71610070880 | 180 TABLET, FILM COATED in 1 BOTTLE (71610-708-80) | 2023-05-16 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Bupropion Hydrochloride | Aphena Pharma Solutions - Tennessee, LLC | 2023-05-16 | HUMAN PRESCRIPTION DRUG LABEL | 1 |