Azithromycin
- Product NDC
- 50090-3213
- 11-digit product format
- 500903213
- Labeler code
- 50090
- Product ID
- 50090-3213_068ab490-e7ae-43c9-b3cc-6602be9ccda8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065225
- Marketing category
- ANDA
- Marketing start
- 2006-01-06
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN DIHYDRATE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Macrolide Antimicrobial [EPC],Macrolides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 50090-3213-0 | Azithromycin | 4 in 1 BOTTLE | TABLET, FILM COATED | 4 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3213 | AZITHROMYCIN TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 7 | Legacy NDC, 1 package rows | 20190404_2c8c977f-6acf-40f9-8a5b-253eb0188ed2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-3213-0 | 50090321300 | 4 in 1 BOTTLE | Historical |