Azithromycin Monohydrate
- Product NDC
- 60687-314
- 11-digit product format
- 606870314
- Labeler code
- 60687
- Product ID
- 60687-314_ea3f6d5b-ef1b-4ffa-e053-2995a90aeab6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin Monohydrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA065400
- Marketing category
- ANDA
- Marketing start
- 2017-07-01
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-314-25 | 60687031425 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-314-25) > 1 TABLET in 1 BLISTER PACK (60687-314-95) | 30 blister pack | 2017-07-01 | 0000-00-00 | No | No | Current |