Azithromycin Dihydrate
- Product NDC
- 72789-169
- 11-digit product format
- 727890169
- Labeler code
- 72789
- Product ID
- 72789-169_e660c56a-d1d6-3c4a-e053-2995a90a7444
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin Dihydrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA208249
- Marketing category
- ANDA
- Marketing start
- 2019-07-01
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN DIHYDRATE
- Active strength
- 500 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
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-169 | AZITHROMYCIN DIHYDRATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.] | 8 | Legacy NDC | 20250328_e73e2f75-a67d-41f9-a4e6-bd74ef3d24b2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-169-30 | 72789016930 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-169-30) | 2021-03-12 | 0000-00-00 | No | No | Current |