Bupropion HCL
NDC 72189-457, Bupropion HCL, tablet, film coated, from Direct_Rx.
- Product NDC
- 72189-457
- Status
- Listed
- Labeler
- Direct_Rx
- 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/72189-457 \ -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 |
|---|---|---|
| 72189-457-30 | 72189045730 | 30 TABLET, FILM COATED in 1 BOTTLE (72189-457-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f820ad7d-3c88-4a4f-e053-6294a90aef7b
Use it
Look up 72189-457 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72189-457 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72189-457. 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.