Package 80425-0219-1
Brand: azithromycin
Generic: azithromycinPackage Facts
Identity
Package NDC
80425-0219-1
Digits Only
8042502191
Product NDC
80425-0219
Description
1 BLISTER PACK in 1 CARTON (80425-0219-1) / 6 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
azithromycin
Generic
azithromycin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a9aa22e-db40-217b-e063-6294a90a4c41", "openfda": {"unii": ["JTE4MNN1MD"], "rxcui": ["308460", "749783"], "spl_set_id": ["f175496a-4ad3-ce0d-e053-2a95a90a6613"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (80425-0219-1) / 6 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "80425-0219-1", "marketing_start_date": "20230109"}], "brand_name": "Azithromycin", "product_id": "80425-0219_2a9aa22e-db40-217b-e063-6294a90a4c41", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "80425-0219", "generic_name": "Azithromycin", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN MONOHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA065225", "marketing_category": "ANDA", "marketing_start_date": "20230109", "listing_expiration_date": "20261231"}