Azithromycin
- Product NDC
- 63187-594
- 11-digit product format
- 631870594
- Labeler code
- 63187
- Product ID
- 63187-594_1b1d0591-dd31-435d-801a-6e7c98c86e51
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA065405
- Marketing category
- ANDA
- Marketing start
- 2008-02-11
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN ANHYDROUS
- Active strength
- 500 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-594 | AZITHROMYCIN TABLET, FILM COATED [PROFICIENT RX LP] | 3 | Legacy NDC | 20210113_8146ad4f-fd84-4414-a899-b7ddd4a63bb5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-594-03 | 63187059403 | 3 TABLET, FILM COATED in 1 BLISTER PACK (63187-594-03) | 2018-12-01 | 0000-00-00 | No | No | Current |