Azithromycin
- Product NDC
- 70518-0193
- 11-digit product format
- 705180193
- Labeler code
- 70518
- Product ID
- 70518-0193_82ce8485-0fa5-1b9d-e053-2991aa0a4783
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065211
- Marketing category
- ANDA
- Marketing start
- 2017-02-02
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN MONOHYDRATE
- 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