Bupropion hydrochloride
NDC 71335-2649, Bupropion hydrochloride, tablet, extended release, from Bryant Ranch Prepack.
- Product NDC
- 71335-2649
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA216800
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2649 \ -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 |
|---|---|---|
| 71335-2649-1 | 71335264901 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-1) |
| 71335-2649-2 | 71335264902 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-2) |
| 71335-2649-3 | 71335264903 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-3) |
| 71335-2649-4 | 71335264904 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-4) |
| 71335-2649-5 | 71335264905 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-5) |
| 71335-2649-6 | 71335264906 | 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-6) |
| 71335-2649-7 | 71335264907 | 21 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2649-7) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/c5d55b0c-8b81-476a-994e-1989e2a56255
Use it
Look up 71335-2649 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2649 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-2649. 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.