bupropion Hydrochloride
- Product NDC
- 0615-8261
- 11-digit product format
- 006158261
- Labeler code
- 0615
- Product ID
- 0615-8261_204c61a5-77c4-4f33-b31c-2e3416b16209
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bupropion Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- 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
- 2023-12-31
- 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 |
|---|
| 0615-8261 | BUPROPION HYDROCHLORIDE TABLET [NCS HEALTHCARE OF KY, LLC DBA VANGARD LABS] | 18 | Legacy NDC | 20250504_ded7a10e-7266-4120-bba3-e5a6b9217a56.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8261-39 | 00615826139 | 30 TABLET in 1 BLISTER PACK (0615-8261-39) | 30 tablet | 2019-01-08 | 0000-00-00 | No | No | Current |