Zithromax
- Product NDC
- 55154-2713
- 11-digit product format
- 551542713
- Labeler code
- 55154
- Product ID
- 55154-2713_e7667374-aebd-4944-9ad1-ba1d58a814cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- NDA050711
- Marketing category
- NDA
- Marketing start
- 1996-07-18
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN DIHYDRATE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Macrolide Antimicrobial [EPC],Macrolides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record