bupropion hydrochloride
NDC 71335-3153, bupropion hydrochloride, tablet, extended release, from Bryant Ranch Prepack.
- Product NDC
- 71335-3153
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211020
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3153 \ -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 |
|---|---|---|
| 71335-3153-1 | 71335315301 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3153-1) |
| 71335-3153-2 | 71335315302 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3153-2) |
| 71335-3153-3 | 71335315303 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3153-3) |
| 71335-3153-4 | 71335315304 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3153-4) |
| 71335-3153-5 | 71335315305 | 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3153-5) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/a613cfd3-1aa1-49c5-b742-b105c97d73f1
Use it
Look up 71335-3153 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3153 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-3153. 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.