Azithromycin Dihydrate
- Product NDC
- 72789-063
- 11-digit product format
- 727890063
- Labeler code
- 72789
- Product ID
- 72789-063_e61085ca-1e1a-5e93-e053-2a95a90a25f2
- 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 |
|---|
| 72789-063 | AZITHROMYCIN DIHYDRATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.] | 7 | Legacy NDC | 20250328_4f5f4a4e-6c86-41f4-8506-14573b5fdfe8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-063-02 | 72789006302 | 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-063-02) | 2020-03-23 | 0000-00-00 | No | No | Current |