Azithromycin
- Product NDC
- 70518-2562
- 11-digit product format
- 705182562
- Labeler code
- 70518
- Product ID
- 70518-2562_ca3b3b52-71ff-4b55-e053-2995a90a1ac1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA210000
- Marketing category
- ANDA
- Marketing start
- 2020-02-04
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN DIHYDRATE
- Active strength
- 250 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
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 |
|---|
| 70518-2562-0 | 70518256200 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2562-0) | 2020-02-04 | 0000-00-00 | No | No | Current |
| 70518-2562-1 | 70518256201 | 6 TABLET, FILM COATED in 1 BLISTER PACK (70518-2562-1) | 2020-02-17 | 0000-00-00 | No | No | Current |
| 70518-2562-2 | 70518256202 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2562-2) | 2020-03-04 | 0000-00-00 | No | No | Current |