Bupropion hydrochloride
NDC 68788-8769, Bupropion hydrochloride, tablet, extended release, from Preferred Pharmaceuticals Inc..
- Product NDC
- 68788-8769
- Status
- Listed
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA216800
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8769 \ -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 |
|---|---|---|
| 68788-8769-1 | 68788876901 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-1) |
| 68788-8769-2 | 68788876902 | 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-2) |
| 68788-8769-3 | 68788876903 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-3) |
| 68788-8769-6 | 68788876906 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-6) |
| 68788-8769-8 | 68788876908 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-8) |
| 68788-8769-9 | 68788876909 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8769-9) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/093c4a61-02d9-4b55-b612-569aa25d3f2a
Use it
Look up 68788-8769 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8769 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68788-8769. 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.