Azithromycin Dihydrate
- Product NDC
- 0527-2750
- 11-digit product format
- 005272750
- Labeler code
- 0527
- Product ID
- 0527-2750_a37530e9-d907-3807-e053-2995a90a3f30
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azithromycin Dihydrate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Marketing category
- UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
- Marketing start
- 2020-04-18
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0527-2750-17 | 00527275017 | 1 BLISTER PACK in 1 CARTON (0527-2750-17) > 3 TABLET, COATED in 1 BLISTER PACK | 1 blister pack | 2020-04-18 | 0000-00-00 | No | No | Current |