Bupropion Hydrochloride XL
NDC 71335-2378, bupropion hydrochloride, tablet, extended release, from Bryant Ranch Prepack.
- Product NDC
- 71335-2378
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210015
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2378 \ -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 |
|---|---|---|
| 71335-2378-1 | 71335237801 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-1) |
| 71335-2378-2 | 71335237802 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-2) |
| 71335-2378-3 | 71335237803 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-3) |
| 71335-2378-4 | 71335237804 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-4) |
| 71335-2378-5 | 71335237805 | 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2378-5) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/eb25adb1-9841-42ce-aa22-718fb0fba5dd
Use it
Look up 71335-2378 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2378 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-2378. 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.