Azithromycin
- Product NDC
- 43063-700
- 11-digit product format
- 430630700
- Labeler code
- 43063
- Product ID
- 43063-700_adcbd68a-3c76-0dfb-e053-2995a90a0d79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA065212
- Marketing category
- ANDA
- Marketing start
- 2005-11-14
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN MONOHYDRATE
- Active strength
- 500 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 |
|---|
| 43063-700-02 | 43063070002 | 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-700-02) | 2016-08-04 | 0000-00-00 | No | No | Current |