Azithromycin
- Product NDC
- 68788-7066
- 11-digit product format
- 687887066
- Labeler code
- 68788
- Product ID
- 68788-7066_392be6bb-f4bf-4df6-a76c-ba5c9b0e5e7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065211
- Marketing category
- ANDA
- Marketing start
- 2018-01-03
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN MONOHYDRATE
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7066-6 | 68788706606 | 6 DOSE PACK in 1 CARTON (68788-7066-6) > 1 TABLET, FILM COATED in 1 DOSE PACK | 6 dose pack | 2018-01-03 | 0000-00-00 | No | No | Current |