Azithromycin
- Product NDC
- 70518-0713
- 11-digit product format
- 705180713
- Labeler code
- 70518
- Product ID
- 70518-0713_e21d3ea1-51ab-777e-e053-2a95a90af2ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065218
- Marketing category
- ANDA
- Marketing start
- 2017-08-25
- 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
- 2023-12-31
- 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 |
|---|
| 70518-0713-0 | 70518071300 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0713-0) | 2017-08-25 | 0000-00-00 | No | No | Current |