Azithromycin
- Product NDC
- 68788-7507
- 11-digit product format
- 687887507
- Labeler code
- 68788
- Product ID
- 68788-7507_ad49432c-1014-471d-a7db-a81b67b7abc5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA207370
- Marketing category
- ANDA
- Marketing start
- 2018-07-05
- 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
- 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 |
|---|
| 68788-7507-6 | 68788750706 | 1 BLISTER PACK in 1 CARTON (68788-7507-6) > 6 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2019-10-25 | 0000-00-00 | No | No | Current |