Bupropion Hydrochloride SR
NDC 71335-1702, bupropion hydrochloride, tablet, film coated, extended release, from Bryant Ranch Prepack.
- Product NDC
- 71335-1702
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA205794
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1702 \ -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 |
|---|---|---|
| 71335-1702-1 | 71335170201 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-1) |
| 71335-1702-2 | 71335170202 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-2) |
| 71335-1702-3 | 71335170203 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-3) |
| 71335-1702-4 | 71335170204 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-4) |
| 71335-1702-5 | 71335170205 | 45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-5) |
| 71335-1702-6 | 71335170206 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-6) |
| 71335-1702-7 | 71335170207 | 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-7) |
| 71335-1702-8 | 71335170208 | 56 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-8) |
| 71335-1702-9 | 71335170209 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1702-9) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/a72db723-df4b-4bf4-9bdc-05ae82058696
Use it
Look up 71335-1702 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-1702 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-1702. 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.