Package 80425-0412-1

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 80425-0412-1
Digits Only 8042504121
Product NDC 80425-0412
Product ID 80425-0412_1d0e96cf-245e-cfb7-e063-6294a90a4ced
Description

1 BLISTER PACK in 1 CARTON (80425-0412-1) / 3 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-07-10
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": "1d0e96cf-245e-cfb7-e063-6294a90a4ced", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "749780"], "spl_set_id": ["1cec44fa-9597-3e58-e063-6394a90ae326"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (80425-0412-1)  / 3 TABLET in 1 BLISTER PACK", "package_ndc": "80425-0412-1", "marketing_start_date": "20240710"}], "brand_name": "azithromycin dihydrate", "product_id": "80425-0412_1d0e96cf-245e-cfb7-e063-6294a90a4ced", "dosage_form": "TABLET", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "80425-0412", "generic_name": "azithromycin dihydrate", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "azithromycin dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA065399", "marketing_category": "ANDA", "marketing_start_date": "20240710", "listing_expiration_date": "20261231"}