Azithromycin
- Product NDC
- 68071-4364
- 11-digit product format
- 680714364
- Labeler code
- 68071
- Product ID
- 68071-4364_bb7b9713-0db5-9785-e053-2995a90ae144
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
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 |
|---|
| 68071-4364-3 | 68071436403 | 3 TABLET, FILM COATED in 1 BLISTER PACK (68071-4364-3) | 2018-03-30 | 0000-00-00 | No | No | Current |