bupropion Hydrochloride
- Product NDC
- 68071-4961
- 11-digit product format
- 680714961
- Labeler code
- 68071
- Product ID
- 68071-4961_bb9f9400-0b87-6bd0-e053-2995a90a7b51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA206975
- Marketing category
- ANDA
- Marketing start
- 2016-08-19
- 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
- 2022-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4961-2 | 68071496102 | 20 TABLET in 1 BOTTLE (68071-4961-2) | 20 tablet | 2019-07-09 | 0000-00-00 | No | No | Current |