azithromycin
- Product NDC
- 0527-2381
- 11-digit product format
- 005272381
- Labeler code
- 0527
- Product ID
- 0527-2381_d11c1841-db17-35b3-e053-2995a90a3c82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AZITHROMYCIN MONOHYDRATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA209043
- Marketing category
- ANDA
- Marketing start
- 2020-04-10
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN MONOHYDRATE
- Active strength
- 600 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0527-2381-32 | 00527238132 | 30 TABLET, FILM COATED in 1 BOTTLE (0527-2381-32) | 2020-04-10 | 0000-00-00 | No | No | Current |