Azithromycin
- Product NDC
- 61442-403
- 11-digit product format
- 614420403
- Labeler code
- 61442
- Product ID
- 61442-403_c0ac4558-23ce-912b-e053-2995a90a8e64
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Carlsbad Technology, Inc.
- Application
- ANDA211318
- Marketing category
- ANDA
- Marketing start
- 2021-04-23
- 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
- 2022-12-31
- 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 |
|---|
| 61442-403-30 | 61442040330 | 30 TABLET, FILM COATED in 1 BOTTLE (61442-403-30) | 2021-04-23 | 0000-00-00 | No | No | Current |