Azithromycin
- Product NDC
- 70518-0353
- 11-digit product format
- 705180353
- Labeler code
- 70518
- Product ID
- 70518-0353_83d6e2a8-4749-192e-e053-2991aa0ad5df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065153
- Marketing category
- ANDA
- Marketing start
- 2017-03-23
- 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