Azithromycin
- Product NDC
- 71335-1252
- 11-digit product format
- 713351252
- Labeler code
- 71335
- Product ID
- 71335-1252_72757355-b62e-4179-b8ee-79cbb414313d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA207398
- Marketing category
- ANDA
- Marketing start
- 2018-07-05
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1252-1 | 71335125201 | 2 TABLET, FILM COATED in 1 BOTTLE (71335-1252-1) | 2022-02-09 | 0000-00-00 | No | No | Current |