Bupropion Hydrochloride
NDC 85534-0006, Bupropion Hydrochloride, tablet, extended release, from HAWAII REPACK, INC..
- Product NDC
- 85534-0006
- Status
- Listed
- Labeler
- HAWAII REPACK, INC.
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077285
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/85534-0006 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUPROPION HYDROCHLORIDE300 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 |
|---|---|---|
| 85534-0006-1 | 85534000601 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-1) |
| 85534-0006-3 | 85534000603 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-3) |
| 85534-0006-5 | 85534000605 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-5) |
| 85534-0006-6 | 85534000606 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-6) |
| 85534-0006-9 | 85534000609 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (85534-0006-9) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/b4a1d3b8-afcf-47e3-96d3-469d8f408a31
Use it
Look up 85534-0006 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/85534-0006 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 85534-0006. 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.