Azithromycin Dihydrate
- Product NDC
- 67046-1502
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin Dihydrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA208250
- Marketing category
- ANDA
- Substance
- AZITHROMYCIN DIHYDRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 67046-1502-3 | 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1502-3) | 2025-01-28 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Azithromycin Dihydrate | Coupler LLC | 2025-01-28 | HUMAN PRESCRIPTION DRUG LABEL | 1 |