Package 72189-090-02
Brand: azithromycin dihydrate
Generic: azithromycin dihydratePackage Facts
Identity
Package NDC
72189-090-02
Digits Only
7218909002
Product NDC
72189-090
Description
2 TABLET, FILM COATED in 1 BOX (72189-090-02)
Marketing
Marketing Status
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": "2be8149b-0d04-e882-e063-6394a90a5b86", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "749780"], "spl_set_id": ["a6426d5f-5518-3c69-e053-2995a90af50f"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOX (72189-090-02)", "package_ndc": "72189-090-02", "marketing_start_date": "20200522"}, {"sample": false, "description": "3 TABLET, FILM COATED in 1 BOX (72189-090-03)", "package_ndc": "72189-090-03", "marketing_start_date": "20200522"}], "brand_name": "AZITHROMYCIN DIHYDRATE", "product_id": "72189-090_2be8149b-0d04-e882-e063-6394a90a5b86", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "72189-090", "generic_name": "AZITHROMYCIN DIHYDRATE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AZITHROMYCIN DIHYDRATE", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA208249", "marketing_category": "ANDA", "marketing_start_date": "20200522", "listing_expiration_date": "20261231"}