Bupropion Hydrochloride
- Product NDC
- 66267-700
- 11-digit product format
- 662670700
- Labeler code
- 66267
- Product ID
- 66267-700_9caf8590-f6df-c959-e053-2995a90ab836
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076143
- Marketing category
- ANDA
- Marketing start
- 2006-01-17
- 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
- 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 |
|---|
| 66267-700-20 | 66267070020 | 20 TABLET, FILM COATED in 1 BOTTLE (66267-700-20) | 2017-10-16 | 0000-00-00 | No | No | Current |
| 66267-700-30 | 66267070030 | 30 TABLET, FILM COATED in 1 BOTTLE (66267-700-30) | 2017-10-16 | 0000-00-00 | No | No | Current |
| 66267-700-60 | 66267070060 | 60 TABLET, FILM COATED in 1 BOTTLE (66267-700-60) | 2017-10-16 | 0000-00-00 | No | No | Current |
| 66267-700-91 | 66267070091 | 120 TABLET, FILM COATED in 1 BOTTLE (66267-700-91) | 2017-10-16 | 0000-00-00 | No | No | Current |