Package 76420-046-06

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 76420-046-06
Digits Only 7642004606
Product NDC 76420-046
Product ID 76420-046_ae7775dd-3ddd-58b8-e053-2995a90ad046
Description

6 TABLET, FILM COATED in 1 BLISTER PACK (76420-046-06)

Marketing

Marketing Status
Marketed Since 2020-09-04
Brand azithromycin dihydrate
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (1)

Azithromycin Dihydrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ae7775dd-3ddd-58b8-e053-2995a90ad046", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["b08bd8fc-20da-4623-9211-ae669452b16d"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BLISTER PACK (76420-046-06)", "package_ndc": "76420-046-06", "marketing_start_date": "20200904"}], "brand_name": "Azithromycin Dihydrate", "product_id": "76420-046_ae7775dd-3ddd-58b8-e053-2995a90ad046", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "76420-046", "generic_name": "Azithromycin Dihydrate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA208250", "marketing_category": "ANDA", "marketing_start_date": "20190701", "listing_expiration_date": "20261231"}