bupropion Hydrochloride
- Product NDC
- 68788-7319
- 11-digit product format
- 687887319
- Labeler code
- 68788
- Product ID
- 68788-7319_da160a74-43f9-4b83-a4a7-d4333a12e678
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA207389
- Marketing category
- ANDA
- Marketing start
- 2019-01-15
- 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
- 2022-12-31
- 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 |
|---|
| 68788-7319-1 | 68788731901 | 100 TABLET in 1 BOTTLE (68788-7319-1) | 100 tablet | 2019-01-15 | 0000-00-00 | No | No | Current |
| 68788-7319-3 | 68788731903 | 30 TABLET in 1 BOTTLE (68788-7319-3) | 30 tablet | 2019-01-15 | 0000-00-00 | No | No | Current |
| 68788-7319-6 | 68788731906 | 60 TABLET in 1 BOTTLE (68788-7319-6) | 60 tablet | 2019-01-15 | 0000-00-00 | No | No | Current |
| 68788-7319-8 | 68788731908 | 120 TABLET in 1 BOTTLE (68788-7319-8) | 120 tablet | 2019-01-15 | 0000-00-00 | No | No | Current |
| 68788-7319-9 | 68788731909 | 90 TABLET in 1 BOTTLE (68788-7319-9) | 90 tablet | 2019-01-15 | 0000-00-00 | No | No | Current |