Azithromycin
- Product NDC
- 55700-852
- 11-digit product format
- 557000852
- Labeler code
- 55700
- Product ID
- 55700-852_2ff0078c-5dc6-4398-95b4-6b175fab6064
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA207370
- Marketing category
- ANDA
- Marketing start
- 2020-03-20
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-852-06 | 55700085206 | 6 TABLET, FILM COATED in 1 BLISTER PACK (55700-852-06) | 2020-03-20 | 0000-00-00 | No | No | Current |