Azithromycin
- Product NDC
- 50268-099
- 11-digit product format
- 502680099
- Labeler code
- 50268
- Product ID
- 50268-099_a40bdf2c-7bcf-121a-e053-2a95a90a963b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA065405
- Marketing category
- ANDA
- Marketing start
- 2018-04-19
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN ANHYDROUS
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-099-13 | 50268009913 | 30 BLISTER PACK in 1 BOX (50268-099-13) > 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-099-11) | 30 blister pack | 2018-04-19 | 0000-00-00 | No | No | Current |