Azithromycin Dihydrate
- Product NDC
- 55700-896
- 11-digit product format
- 557000896
- Labeler code
- 55700
- Product ID
- 55700-896_dbc75f46-32bd-4fc0-89ac-b08025c11cac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin Dihydrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA208249
- Marketing category
- ANDA
- Marketing start
- 2021-01-20
- 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
- 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 |
|---|
| 55700-896-03 | 55700089603 | 1 BLISTER PACK in 1 CARTON (55700-896-03) > 3 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2021-01-20 | 0000-00-00 | No | No | Current |