Bupropion hydrochloride
NDC 71335-2469, Bupropion hydrochloride, tablet, extended release, from Bryant Ranch Prepack.
- Product NDC
- 71335-2469
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215568
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2469 \ -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 |
|---|---|---|
| 71335-2469-1 | 71335246901 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-1) |
| 71335-2469-2 | 71335246902 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-2) |
| 71335-2469-3 | 71335246903 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-3) |
| 71335-2469-4 | 71335246904 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-4) |
| 71335-2469-5 | 71335246905 | 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-5) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/af5b1cc8-f078-4a7b-b64a-4cb2de1e5721
Use it
Look up 71335-2469 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2469 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-2469. 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.