azithromycin
- Product NDC
- 55700-211
- 11-digit product format
- 557000211
- Labeler code
- 55700
- Product ID
- 55700-211_6cdfbc8b-abeb-4522-b973-ccfceabf4c91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- azithromycin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- NDA050710
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1995-10-19
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN DIHYDRATE
- Active strength
- 200 mg/5mL
- Pharmacologic classes
- Macrolide Antimicrobial [EPC],Macrolides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record