Azithromycin Dihydrate
- Product NDC
- 55700-859
- 11-digit product format
- 557000859
- Labeler code
- 55700
- Product ID
- 55700-859_33bb3b24-34f8-4b38-a860-1a5a8d8aa226
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin Dihydrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA208250
- Marketing category
- ANDA
- Marketing start
- 2020-05-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-859-06 | 55700085906 | 6 TABLET, FILM COATED in 1 BOTTLE (55700-859-06) | 2020-05-01 | 0000-00-00 | No | No | Current |