Azithromycin
- Product NDC
- 63629-8311
- 11-digit product format
- 636298311
- Labeler code
- 63629
- Product ID
- 63629-8311_000aa40a-90bc-4ea1-b942-3dfb063d52ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210000
- Marketing category
- ANDA
- Marketing start
- 2019-03-12
- Marketing end
- 0000-00-00
- Substance
- AZITHROMYCIN DIHYDRATE
- Active strength
- 250 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8311-1 | 63629831101 | 6 TABLET, FILM COATED in 1 BOTTLE (63629-8311-1) | 2019-03-12 | 0000-00-00 | No | No | Current |