Package 80425-0218-1

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 80425-0218-1
Digits Only 8042502181
Product NDC 80425-0218
Description

1 BLISTER PACK in 1 BOX (80425-0218-1) / 6 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-01-09
Brand azithromycin dihydrate
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a9aa671-d0a1-2254-e063-6294a90a9f79", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["f1752913-85ac-01fa-e053-2995a90a2bd8"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 BOX (80425-0218-1)  / 6 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "80425-0218-1", "marketing_start_date": "20230109"}], "brand_name": "Azithromycin Dihydrate", "product_id": "80425-0218_2a9aa671-d0a1-2254-e063-6294a90a9f79", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "80425-0218", "generic_name": "Azithromycin Dihydrate", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "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": "20230109", "listing_expiration_date": "20261231"}