Bupropion Hydrochloride
NDC 71610-774, Bupropion Hydrochloride, tablet, film coated, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-774
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- 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/71610-774 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUPROPION HYDROCHLORIDE75 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 |
|---|---|---|
| 71610-774-53 | 71610077453 | 60 TABLET, FILM COATED in 1 BOTTLE (71610-774-53) |
| 71610-774-70 | 71610077470 | 120 TABLET, FILM COATED in 1 BOTTLE (71610-774-70) |
| 71610-774-80 | 71610077480 | 180 TABLET, FILM COATED in 1 BOTTLE (71610-774-80) |
| 71610-774-94 | 71610077494 | 360 TABLET, FILM COATED in 1 BOTTLE (71610-774-94) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/8d80f882-1887-4d73-b09f-e98fd7ef2acb
Use it
Look up 71610-774 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-774 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-774. 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.