Azithromycin
NDC 76420-589, Azithromycin, tablet, film coated, from Asclemed USA, Inc..
- Product NDC
- 76420-589
- Status
- Listed
- Labeler
- Asclemed USA, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA065223
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/76420-589 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- AZITHROMYCIN MONOHYDRATE500 mg/1
Pharmacologic classes
Macrolide Antimicrobial [EPC]; Macrolides [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 76420-589-03 | 76420058903 | 3 TABLET, FILM COATED in 1 BLISTER PACK (76420-589-03) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9c44af6d-8a9a-cb4c-e053-2a95a90afdac
Use it
Look up 76420-589 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/76420-589 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 76420-589. 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.