Bupropion Hydrochloride
- Product NDC
- 68788-7174
- 11-digit product format
- 687887174
- Labeler code
- 68788
- Product ID
- 68788-7174_5b23c96d-80b5-4862-8bcd-e9a8a5667f06
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA205794
- Marketing category
- ANDA
- Marketing start
- 2018-08-14
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 200 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 |
|---|
| 68788-7174-1 | 68788717401 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7174-1) | 2018-08-14 | 0000-00-00 | No | No | Current |
| 68788-7174-2 | 68788717402 | 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7174-2) | 2018-08-14 | 0000-00-00 | No | No | Current |
| 68788-7174-3 | 68788717403 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7174-3) | 2018-08-14 | 0000-00-00 | No | No | Current |
| 68788-7174-6 | 68788717406 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7174-6) | 2018-08-14 | 0000-00-00 | No | No | Current |
| 68788-7174-8 | 68788717408 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7174-8) | 2018-08-14 | 0000-00-00 | No | No | Current |
| 68788-7174-9 | 68788717409 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7174-9) | 2018-08-14 | 0000-00-00 | No | No | Current |