Bupropion hydrochloride
NDC 0615-8602, Bupropion hydrochloride, tablet, extended release, from NCS HealthCare of KY, LLC dba Vangard Labs.
- Product NDC
- 0615-8602
- Status
- Listed
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA216800
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8602 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUPROPION HYDROCHLORIDE150 mg/1
Pharmacologic classes
Aminoketone [EPC]; Dopamine Uptake Inhibitors [MoA]; Increased Dopamine Activity [PE]; Increased Norepinephrine Activity [PE]; Norepinephrine Uptake Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0615-8602-39 | 00615860239 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8602-39) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/1bd2ed35-35c5-464f-bf51-9dd4b42ee59a
Use it
Look up 0615-8602 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8602 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0615-8602. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.