BUPROPION HYDROCHLORIDE
NDC 42806-411, BUPROPION HYDROCHLORIDE, tablet, extended release, from Epic Pharma LLC.
- Product NDC
- 42806-411
- Status
- Listed
- Labeler
- Epic Pharma LLC
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075932
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42806-411 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUPROPION HYDROCHLORIDE200 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 |
|---|---|---|
| 42806-411-60 | 42806041160 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-411-60) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/9fb44e96-6160-4a4a-90cb-91764c0dcd89
Use it
Look up 42806-411 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42806-411 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42806-411. 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.