Package 72189-087-06

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 72189-087-06
Digits Only 7218908706
Product NDC 72189-087
Description

6 TABLET, FILM COATED in 1 BOTTLE (72189-087-06)

Marketing

Marketing Status
Marketed Since 2020-06-15
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": "26f851bf-1b84-d000-e063-6394a90a079c", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "308460", "749780", "749783"], "spl_set_id": ["a5b4092d-ab72-f5d1-e053-2995a90ac582"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (72189-087-06)", "package_ndc": "72189-087-06", "marketing_start_date": "20200615"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (72189-087-10)", "package_ndc": "72189-087-10", "marketing_start_date": "20200615"}], "brand_name": "AZITHROMYCIN", "product_id": "72189-087_26f851bf-1b84-d000-e063-6394a90a079c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "72189-087", "generic_name": "AZITHROMYCIN", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AZITHROMYCIN", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA207370", "marketing_category": "ANDA", "marketing_start_date": "20200615", "listing_expiration_date": "20261231"}