Azithromycin
- Product NDC
- 55700-785
- 11-digit product format
- 557000785
- Labeler code
- 55700
- Product ID
- 55700-785_164654c5-5d29-4910-b873-f58e13aaf1f3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA065211
- Marketing category
- ANDA
- Marketing start
- 2019-08-30
- 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
FDA-Initiated Inactive NDC Indexing#