BUPROPION HYDROCHLORIDE
- Product NDC
- 71205-504
- 11-digit product format
- 712050504
- Labeler code
- 71205
- Product ID
- 71205-504_8ab86beb-3616-414c-92bf-25273a853a9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUPROPION HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA210497
- Marketing category
- ANDA
- Marketing start
- 2018-11-08
- 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
- 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 |
|---|
| 71205-504-30 | 71205050430 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-30) | 2020-11-13 | No | No | Historical |
| 71205-504-60 | 71205050460 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-60) | 2020-11-13 | No | No | Historical |
| 71205-504-90 | 71205050490 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-90) | 2020-11-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| BUPROPION HYDROCHLORIDE | Proficient Rx LP | 2022-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |