Azithromycin
- Product NDC
- 63187-622
- 11-digit product format
- 631870622
- Labeler code
- 63187
- Product ID
- 63187-622_788b4191-969a-4aa1-b043-2db763575d22
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA065212
- Marketing category
- ANDA
- Marketing start
- 2005-11-14
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN MONOHYDRATE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Macrolide Antimicrobial [EPC],Macrolides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-622 | AZITHROMYCIN TABLET, FILM COATED [PROFICIENT RX LP] | 3 | Legacy NDC | 20191121_9a2d1be5-ee03-4af9-8f9d-eb3cb06c71c6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-622-03 | 63187062203 | 3 TABLET, FILM COATED in 1 DOSE PACK (63187-622-03) | 2018-12-01 | 0000-00-00 | No | No | Current |