Bupropion Hydrochloride
NDC 71335-0182, Bupropion Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-0182
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076143
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0182 \ -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 |
|---|---|---|
| 71335-0182-1 | 71335018201 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0182-1) |
| 71335-0182-2 | 71335018202 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0182-2) |
| 71335-0182-3 | 71335018203 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0182-3) |
| 71335-0182-4 | 71335018204 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0182-4) |
| 71335-0182-5 | 71335018205 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0182-5) |
| 71335-0182-6 | 71335018206 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0182-6) |
| 71335-0182-7 | 71335018207 | 21 TABLET, FILM COATED in 1 BOTTLE (71335-0182-7) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2a13267f-c47f-4791-a8f9-4bbb5c804027
Use it
Look up 71335-0182 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0182 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-0182. 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.