Azithromycin
- Product NDC
- 50090-4721
- 11-digit product format
- 500904721
- Labeler code
- 50090
- Product ID
- 50090-4721_557a7cc9-f9e4-46df-9d45-8be9093edf27
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207370
- Marketing category
- ANDA
- Marketing start
- 2018-07-05
- Substance
- AZITHROMYCIN DIHYDRATE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Macrolide Antimicrobial [EPC], Macrolides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5FD1131I7S | AZITHROMYCIN DIHYDRATE | 117772-70-0 | AZITHROMYCIN DIHYDRATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-4721-3 | 50090472103 | 3 BLISTER PACK in 1 CARTON (50090-4721-3) / 6 TABLET, FILM COATED in 1 BLISTER PACK | 3 blister pack | 2020-01-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Azithromycin | A-S Medication Solutions | 2024-06-12 | Human Prescription Drug Label | 9 |