Azithromycin
- Product NDC
- 63629-7910
- 11-digit product format
- 636297910
- Labeler code
- 63629
- Product ID
- 63629-7910_fcb9f93e-272f-4e4b-aa00-f28b4b69e071
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065211
- Marketing category
- ANDA
- Marketing start
- 2005-11-14
- Marketing end
- 2022-03-28
- Substance
- AZITHROMYCIN MONOHYDRATE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Macrolide Antimicrobial [EPC], Macrolides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 63629-7910-1 | 63629791001 | 6 TABLET, FILM COATED in 1 BOTTLE (63629-7910-1) | 2019-02-22 | 0000-00-00 | No | No | Current |