Bupropion Hydrochloride
- Product NDC
- 63629-3233
- 11-digit product format
- 636293233
- Labeler code
- 63629
- Product ID
- 63629-3233_50450c8c-eac0-4cba-8e34-fdbc53c15e13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bupropion Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075584
- Marketing category
- ANDA
- Marketing start
- 2000-02-07
- Marketing end
- 0000-00-00
- Substance
- BUPROPION HYDROCHLORIDE
- Active strength
- 100 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-3233-1 | 63629323301 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-3233-1) | 2009-10-22 | 0000-00-00 | No | No | Current |
| 63629-3233-2 | 63629323302 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-3233-2) | 2009-10-22 | 0000-00-00 | No | No | Current |
| 63629-3233-3 | 63629323303 | 100 TABLET, FILM COATED in 1 BOTTLE (63629-3233-3) | 2009-10-22 | 0000-00-00 | No | No | Current |
| 63629-3233-4 | 63629323304 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-3233-4) | 2009-10-22 | 0000-00-00 | No | No | Current |
| 63629-3233-5 | 63629323305 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-3233-5) | 2006-09-28 | 0000-00-00 | No | No | Current |
| 63629-3233-6 | 63629323306 | 15 TABLET, FILM COATED in 1 BOTTLE (63629-3233-6) | 2006-09-28 | 0000-00-00 | No | No | Current |