Azithromycin
- Product NDC
- 55695-028
- 11-digit product format
- 556950028
- Labeler code
- 55695
- Product ID
- 55695-028_2dc8a875-7d68-2544-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Department of State Health Services, Pharmacy Branch
- Application
- ANDA065153
- Marketing category
- ANDA
- Marketing start
- 2005-11-16
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN MONOHYDRATE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Macrolide Antimicrobial [EPC],Macrolides [CS]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55695-028-00 | Azithromycin | 6 in 1 BLISTER PACK | TABLET, FILM COATED | 6 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55695-028 | AZITHROMYCIN TABLET, FILM COATED [DEPARTMENT OF STATE HEALTH SERVICES, PHARMACY BRANCH] | 2 | Legacy NDC, 1 package rows | 20160311_2bd73040-8aad-0bce-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55695-028-00 | 55695002800 | 6 in 1 BLISTER PACK | Historical |