azithromycin
- Product NDC
- 68788-9038
- 11-digit product format
- 687889038
- Labeler code
- 68788
- Product ID
- 68788-9038_69b1e05f-1068-4ec7-bf4e-184c04ac19c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- NDA050711
- Marketing category
- NDA AUTHORIZED GENERIC
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record