Bupropion Hydrochloride
- Product NDC
- 63629-2642
- 11-digit product format
- 636292642
- Labeler code
- 63629
- Product ID
- 63629-2642_1ef0458d-d5e2-4b42-9569-2c05cd860e06
- 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
- 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
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 |
|---|
| 63629-2642-1 | 63629264201 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-2642-1) | 2007-03-08 | 0000-00-00 | No | No | Current |