Package 72189-093-06

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 72189-093-06
Digits Only 7218909306
Product NDC 72189-093
Product ID 72189-093_26f851bf-1b84-d000-e063-6394a90a079c
Description

6 TABLET, FILM COATED in 1 BLISTER PACK (72189-093-06)

Marketing

Marketing Status
Marketed Since 2020-05-15
Brand azithromycin
Generic azithromycin
Sample Package No

Linked Drug Pages (1)

AZITHROMYCIN, AZITHROMYCIN DIHYDRATE ndc-match (0.95)

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 BLISTER PACK (72189-093-06)", "package_ndc": "72189-093-06", "marketing_start_date": "20200515"}], "brand_name": "AZITHROMYCIN", "product_id": "72189-093_26f851bf-1b84-d000-e063-6394a90a079c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "72189-093", "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": "ANDA210000", "marketing_category": "ANDA", "marketing_start_date": "20200515", "listing_expiration_date": "20261231"}