Azithromycin
- Product NDC
- 42291-084
- 11-digit product format
- 422910084
- Labeler code
- 42291
- Product ID
- 42291-084_dc63fbf4-40c3-9712-e053-2995a90a66dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA209999
- Marketing category
- ANDA
- Marketing start
- 2022-04-11
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN DIHYDRATE
- Active strength
- 600 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-084-30 | 42291008430 | 30 TABLET, FILM COATED in 1 BOTTLE (42291-084-30) | 2022-04-11 | 0000-00-00 | No | No | Current |