azithromycin
- Product NDC
- 68788-0713
- 11-digit product format
- 687880713
- Labeler code
- 68788
- Product ID
- 68788-0713_2c6acff2-bde2-4262-a67f-565983868ec2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AZITHROMYCIN
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- NDA050693
- Marketing category
- NDA
- Marketing start
- 1999-02-12
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN DIHYDRATE
- Active strength
- 1 g/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 |
|---|
| 68788-0713-1 | 68788071301 | 1 POWDER, FOR SUSPENSION in 1 PACKET (68788-0713-1) | 1999-02-12 | 0000-00-00 | No | No | Current |