azithromycin
- Product NDC
- 76413-101
- 11-digit product format
- 764130101
- Labeler code
- 76413
- Product ID
- 76413-101_a246c0fb-d73d-422a-b849-d4475234dcc4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- azithromycin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Central Texas Community Health Centers
- Application
- NDA050711
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1996-07-18
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76413-101-04 | azithromycin | 4 in 1 BOTTLE | TABLET, FILM COATED | 4 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76413-101 | AZITHROMYCIN TABLET, FILM COATED [CENTRAL TEXAS COMMUNITY HEALTH CENTERS] | 1 | Legacy NDC, 1 package rows | 20160130_794a2a15-24c1-430f-8821-643164c26dbf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 76413-101-04 | 76413010104 | 4 in 1 BOTTLE | Historical |