Bupropion Hydrochloride (XL)
NDC 70518-3963, bupropion hydrochloride, tablet, film coated, extended release, from REMEDYREPACK INC..
- Product NDC
- 70518-3963
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207479
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3963 \ -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 |
|---|---|---|
| 70518-3963-3 | 70518396303 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3963-3) |
| 70518-3963-4 | 70518396304 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3963-4) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/0cd6e0e2-6b2c-4e0d-b5b2-ebfe0d5e31c4
Use it
Look up 70518-3963 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3963 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-3963. 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.