Azithromycin Dihydrate
- Product NDC
- 50090-4602
- 11-digit product format
- 500904602
- Labeler code
- 50090
- Product ID
- 50090-4602_8d6e3fb6-0017-4bb3-8761-9ad3b9145517
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin Dihydrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA208250
- Marketing category
- ANDA
- Marketing start
- 2019-07-01
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4602-2 | 50090460202 | 3 CARTON in 1 BOX (50090-4602-2) > 1 TABLET, FILM COATED in 1 CARTON | 3 carton | 2019-12-06 | 0000-00-00 | No | No | Current |