Azithromycin Dihydrate
- Product NDC
- 50268-076
- 11-digit product format
- 502680076
- Labeler code
- 50268
- Product ID
- 50268-076_ed84e3e2-c85e-eb0c-e053-2995a90a9d14
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin Dihydrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA208249
- Marketing category
- ANDA
- Marketing start
- 2020-12-11
- 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 Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50268-076-11 | Azithromycin Dihydrate | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 8 |
| 50268-076-12 | Azithromycin Dihydrate | 20 in 1 BOX | TABLET, FILM COATED | 20 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50268-076 | AZITHROMYCIN DIHYDRATE TABLET, FILM COATED [AVPAK] | 7 | Legacy NDC, 2 package rows | 20240921_b635019e-7fd4-7f9e-e053-2a95a90a388c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-076-11 | 50268007611 | 1 in 1 BLISTER PACK | | | | | | Historical |
| 50268-076-12 | 50268007612 | 20 BLISTER PACK in 1 BOX (50268-076-12) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-076-11) | 20 blister pack | 2020-12-11 | 0000-00-00 | No | No | Current |