Azithromycin
- Product NDC
- 68071-4774
- 11-digit product format
- 680714774
- Labeler code
- 68071
- Product ID
- 68071-4774_c9f07ae9-1e3f-9cbb-e053-2995a90afaa9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065223
- Marketing category
- ANDA
- Marketing start
- 2006-01-06
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4774-2 | 68071477402 | 2 TABLET, FILM COATED in 1 BOTTLE (68071-4774-2) | 2021-08-19 | 0000-00-00 | No | No | Current |
| 68071-4774-6 | 68071477406 | 6 TABLET, FILM COATED in 1 BOTTLE (68071-4774-6) | 2019-02-19 | 0000-00-00 | No | No | Current |