azithromycin
- Product NDC
- 63629-6764
- 11-digit product format
- 636296764
- Labeler code
- 63629
- Product ID
- 63629-6764_166f9a84-23a7-4a59-bff3-794d824d4611
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA050784
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2002-05-24
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN DIHYDRATE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Macrolide Antimicrobial [EPC],Macrolides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63629-6764-1 | 63629676401 | 2 TABLET, FILM COATED in 1 BOTTLE (63629-6764-1) | 2015-09-15 | 0000-00-00 | No | No | Current |
| 63629-6764-2 | 63629676402 | 14 TABLET, FILM COATED in 1 BOTTLE (63629-6764-2) | 2015-09-15 | 0000-00-00 | No | No | Current |