Bupropion Hydrochloride
- Product NDC
- 60429-933
- 11-digit product format
- 604290933
- Labeler code
- 60429
- Product ID
- 60429-933_b02a5964-ea8a-18e3-e053-2a95a90afd77
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA077715
- Marketing category
- ANDA
- Marketing start
- 2008-11-26
- 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 |
|---|
| 60429-933-05 | 60429093305 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60429-933-05) | 2016-08-26 | 0000-00-00 | No | No | Current |
| 60429-933-30 | 60429093330 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60429-933-30) | 2016-08-26 | 0000-00-00 | No | No | Current |
| 60429-933-90 | 60429093390 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60429-933-90) | 2016-08-26 | 0000-00-00 | No | No | Current |