Bupropion Hydrochloride SR
NDC 50090-6871, bupropion hydrochloride, tablet, film coated, extended release, from A-S Medication Solutions.
- Product NDC
- 50090-6871
- Status
- Listed
- Labeler
- A-S Medication Solutions
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA205794
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50090-6871 \ -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 |
|---|---|---|
| 50090-6871-0 | 50090687100 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-0) |
| 50090-6871-1 | 50090687101 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-1) |
| 50090-6871-2 | 50090687102 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-2) |
| 50090-6871-3 | 50090687103 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6871-3) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/73167de9-948d-465c-88c0-c7743a79e7f5
Use it
Look up 50090-6871 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50090-6871 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50090-6871. 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.