BUPROPION HYDROCHLORIDE
NDC 72189-134, BUPROPION HYDROCHLORIDE, tablet, extended release, from DIRECT RX.
- Product NDC
- 72189-134
- Status
- Listed
- Labeler
- DIRECT RX
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210497
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72189-134 \ -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 |
|---|---|---|
| 72189-134-30 | 72189013430 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-30) |
| 72189-134-60 | 72189013460 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-60) |
| 72189-134-72 | 72189013472 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-72) |
| 72189-134-90 | 72189013490 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-90) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/96d87edc-d12b-44b2-e053-2995a90a4e63
Use it
Look up 72189-134 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72189-134 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72189-134. 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.