Package 80425-0431-1

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 80425-0431-1
Digits Only 8042504311
Product NDC 80425-0431
Product ID 80425-0431_20ae1090-cc58-39fd-e063-6294a90adfab
Description

6 TABLET in 1 BLISTER PACK (80425-0431-1)

Marketing

Marketing Status
Marketed Since 2024-08-27
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": "20ae1090-cc58-39fd-e063-6294a90adfab", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["20ae108a-00c5-a984-e063-6394a90aaaae"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BLISTER PACK (80425-0431-1)", "package_ndc": "80425-0431-1", "marketing_start_date": "20240827"}], "brand_name": "azithromycin dihydrate", "product_id": "80425-0431_20ae1090-cc58-39fd-e063-6294a90adfab", "dosage_form": "TABLET", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "80425-0431", "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": "250 mg/1"}], "application_number": "ANDA065398", "marketing_category": "ANDA", "marketing_start_date": "20240827", "listing_expiration_date": "20261231"}