bupropion Hydrochloride
- Product NDC
- 71335-1192
- 11-digit product format
- 713351192
- Labeler code
- 71335
- Product ID
- 71335-1192_fc929c15-d3b5-46b6-ac26-db87778c7fa5
- 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
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1192-1 | 71335119201 | 60 TABLET in 1 BOTTLE (71335-1192-1) | 60 tablet | 2019-04-22 | 0000-00-00 | No | No | Current |
| 71335-1192-2 | 71335119202 | 30 TABLET in 1 BOTTLE (71335-1192-2) | 30 tablet | 2019-04-22 | 0000-00-00 | No | No | Current |
| 71335-1192-3 | 71335119203 | 100 TABLET in 1 BOTTLE (71335-1192-3) | 100 tablet | 2019-04-22 | 0000-00-00 | No | No | Current |
| 71335-1192-4 | 71335119204 | 90 TABLET in 1 BOTTLE (71335-1192-4) | 90 tablet | 2019-04-22 | 0000-00-00 | No | No | Current |
| 71335-1192-5 | 71335119205 | 120 TABLET in 1 BOTTLE (71335-1192-5) | 120 tablet | 2019-04-22 | 0000-00-00 | No | No | Current |
| 71335-1192-6 | 71335119206 | 15 TABLET in 1 BOTTLE (71335-1192-6) | 15 tablet | 2019-04-22 | 0000-00-00 | No | No | Current |
| 71335-1192-7 | 71335119207 | 21 TABLET in 1 BOTTLE (71335-1192-7) | 21 tablet | 2022-02-23 | 0000-00-00 | No | No | Current |