bupropion Hydrochloride
- Product NDC
- 71335-0943
- 11-digit product format
- 713350943
- Labeler code
- 71335
- Product ID
- 71335-0943_54094d85-96a6-49c2-a58c-4d4fcfb3c0ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207389
- Marketing category
- ANDA
- Marketing start
- 2018-05-26
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 75 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0943-1 | 71335094301 | 30 TABLET in 1 BOTTLE (71335-0943-1) | 30 tablet | 2018-05-26 | 0000-00-00 | No | No | Current |
| 71335-0943-2 | 71335094302 | 60 TABLET in 1 BOTTLE (71335-0943-2) | 60 tablet | 2018-05-26 | 0000-00-00 | No | No | Current |
| 71335-0943-3 | 71335094303 | 90 TABLET in 1 BOTTLE (71335-0943-3) | 90 tablet | 2018-05-26 | 0000-00-00 | No | No | Current |
| 71335-0943-4 | 71335094304 | 7 TABLET in 1 BOTTLE (71335-0943-4) | 7 tablet | 2018-05-26 | 0000-00-00 | No | No | Current |
| 71335-0943-5 | 71335094305 | 14 TABLET in 1 BOTTLE (71335-0943-5) | 14 tablet | 2018-05-26 | 0000-00-00 | No | No | Current |
| 71335-0943-6 | 71335094306 | 120 TABLET in 1 BOTTLE (71335-0943-6) | 120 tablet | 2018-05-26 | 0000-00-00 | No | No | Current |
| 71335-0943-7 | 71335094307 | 100 TABLET in 1 BOTTLE (71335-0943-7) | 100 tablet | 2018-09-05 | 0000-00-00 | No | No | Current |