Package 72189-015-02

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 72189-015-02
Digits Only 7218901502
Product NDC 72189-015
Description

2 TABLET, FILM COATED in 1 BOTTLE (72189-015-02)

Marketing

Marketing Status
Marketed Since 2019-07-24
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": "2c4e8f12-2481-4a0d-e063-6394a90a58c5", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["8e6e11fb-eb9e-28ec-e053-2a95a90aa1a3"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (72189-015-02)", "package_ndc": "72189-015-02", "marketing_start_date": "20190724"}, {"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (72189-015-03)", "package_ndc": "72189-015-03", "marketing_start_date": "20190724"}], "brand_name": "AZITHROMYCIN", "product_id": "72189-015_2c4e8f12-2481-4a0d-e063-6394a90a58c5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "72189-015", "generic_name": "AZITHROMYCIN", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AZITHROMYCIN", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA207398", "marketing_category": "ANDA", "marketing_start_date": "20190724", "listing_expiration_date": "20261231"}