bupropion Hydrochloride
- Product NDC
- 0615-8296
- 11-digit product format
- 006158296
- Labeler code
- 0615
- Product ID
- 0615-8296_ea682f4e-8dce-4696-9931-02a1fd783593
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA206975
- Marketing category
- ANDA
- Marketing start
- 2016-08-19
- 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
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0615-8296 | BUPROPION HYDROCHLORIDE TABLET [NCS HEALTHCARE OF KY, LLC DBA VANGARD LABS] | 18 | Legacy NDC | 20250507_271fff08-3774-4933-b5d6-e8e822519ea1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8296-39 | 00615829639 | 30 TABLET in 1 BLISTER PACK (0615-8296-39) | 30 tablet | 2019-07-02 | 0000-00-00 | No | No | Current |