Bupropion Hydrochloride
- Product NDC
- 68788-6800
- 11-digit product format
- 687886800
- Labeler code
- 68788
- Product ID
- 68788-6800_1b3e1a5b-65e9-4b5d-83a5-b738ade6b370
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUPROPION HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA077415
- Marketing category
- ANDA
- Marketing start
- 2016-10-31
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- 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 |
|---|
| 68788-6800-1 | 68788680001 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6800-1) | 2016-10-31 | 0000-00-00 | No | No | Current |
| 68788-6800-3 | 68788680003 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6800-3) | 2016-10-31 | 0000-00-00 | No | No | Current |
| 68788-6800-6 | 68788680006 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6800-6) | 2016-10-31 | 0000-00-00 | No | No | Current |
| 68788-6800-8 | 68788680008 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6800-8) | 2016-10-31 | 0000-00-00 | No | No | Current |
| 68788-6800-9 | 68788680009 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6800-9) | 2016-10-31 | 0000-00-00 | No | No | Current |