Bupropion Hydrochloride
- Product NDC
- 67544-406
- 11-digit product format
- 675440406
- Labeler code
- 67544
- Product ID
- 67544-406_00ff6c58-e096-4d7a-8e7b-62d98946eac0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA075491
- Marketing category
- ANDA
- Marketing start
- 2000-05-11
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67544-406-51 | 67544040651 | 6000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67544-406-51) | 2014-12-05 | 0000-00-00 | No | No | Current |
| 67544-406-53 | 67544040653 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67544-406-53) | 2016-08-31 | 0000-00-00 | No | No | Current |
| 67544-406-70 | 67544040670 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67544-406-70) | 2016-08-31 | 0000-00-00 | No | No | Current |
| 67544-406-80 | 67544040680 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67544-406-80) | 2014-11-24 | 0000-00-00 | No | No | Current |
| 67544-406-94 | 67544040694 | 360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (67544-406-94) | 2014-11-24 | 0000-00-00 | No | No | Current |