Bupropion Hydrochloride
NDC 50268-143, Bupropion Hydrochloride, tablet, film coated, from AvPAK.
- Product NDC
- 50268-143
- Status
- Listed
- Labeler
- AvPAK
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076143
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50268-143 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUPROPION HYDROCHLORIDE100 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 |
|---|---|---|
| 50268-143-15 | 50268014315 | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-143-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-143-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/bcb4ef83-f272-4090-8547-9aaf4ab63667NADAC price for package 50268014315
GET /v1/drugs/nadac/50268014315
Use it
Look up 50268-143 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50268-143 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50268-143. 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.