Bupropion Hydrochloride
NDC 47335-954, Bupropion Hydrochloride, tablet, extended release, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 47335-954
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA200695
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/47335-954 \ -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 |
|---|---|---|
| 47335-954-13 | 47335095413 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-13) |
| 47335-954-81 | 47335095481 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-81) |
| 47335-954-83 | 47335095483 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-83) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/e4e38abf-ef67-405b-af2d-3d8e4533654d
Use it
Look up 47335-954 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47335-954 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47335-954. 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.