Azithromycin
- Product NDC
- 68788-7659
- 11-digit product format
- 687887659
- Labeler code
- 68788
- Product ID
- 68788-7659_0cfbd326-bff7-425c-9344-a32211196d6f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA210000
- Marketing category
- ANDA
- Marketing start
- 2020-05-01
- 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
- 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 |
|---|
| 68788-7659-6 | 68788765906 | 6 TABLET, FILM COATED in 1 BLISTER PACK (68788-7659-6) | 2020-05-01 | 0000-00-00 | No | No | Current |