AZITHROMYCIN
- Product NDC
- 55700-731
- 11-digit product format
- 557000731
- Labeler code
- 55700
- Product ID
- 55700-731_9fac2856-f510-40a2-ad19-806e7b2aad24
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AZITHROMYCIN
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Quality Care Products LLC
- Application
- ANDA207531
- Marketing category
- ANDA
- Marketing start
- 2019-03-15
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN MONOHYDRATE
- Active strength
- 200 mg/5mL
- Pharmacologic classes
- Macrolide Antimicrobial [EPC], Macrolides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-731-30 | 55700073130 | 30 mL in 1 BOTTLE, PLASTIC (55700-731-30) | 30 ml | 2019-03-15 | 0000-00-00 | No | No | Current |