Bupropion Hydrochloride XL
NDC 63187-766, Bupropion Hydrochloride, tablet, film coated, extended release, from Proficient Rx LP.
- Product NDC
- 63187-766
- Status
- Listed
- Labeler
- Proficient Rx LP
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077715
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/63187-766 \ -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 |
|---|---|---|
| 63187-766-30 | 63187076630 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-766-30) |
| 63187-766-60 | 63187076660 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-766-60) |
| 63187-766-90 | 63187076690 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-766-90) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/ec9cbb38-1582-492f-a526-4b3675c55b14
Use it
Look up 63187-766 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63187-766 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63187-766. 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.