Azithromycin Dihydrate
NDC 80425-0220, Azithromycin Dihydrate, tablet, film coated, from Advanced Rx of Tennessee, LLC.
- Product NDC
- 80425-0220
- Status
- Listed
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208249
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0220 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- AZITHROMYCIN DIHYDRATE500 mg/1
Pharmacologic classes
Macrolide Antimicrobial [EPC]; Macrolides [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 80425-0220-1 | 80425022001 | 1 BLISTER PACK in 1 CARTON (80425-0220-1) / 3 TABLET, FILM COATED in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f1755cf3-bf7f-be40-e053-2a95a90a8536
Use it
Look up 80425-0220 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0220 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 80425-0220. 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.