Package 72189-089-06

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 72189-089-06
Digits Only 7218908906
Product NDC 72189-089
Product ID 72189-089_26f851bf-1b84-d000-e063-6394a90a079c
Description

6 TABLET, FILM COATED in 1 BOTTLE (72189-089-06)

Marketing

Marketing Status
Marketed Since 2020-10-15
Brand azithromycin dihydrate
Generic azithromycin dihydrate
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 BOTTLE (72189-089-06)", "package_ndc": "72189-089-06", "marketing_start_date": "20201015"}], "brand_name": "AZITHROMYCIN DIHYDRATE", "product_id": "72189-089_26f851bf-1b84-d000-e063-6394a90a079c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "72189-089", "generic_name": "AZITHROMYCIN DIHYDRATE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AZITHROMYCIN DIHYDRATE", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA208250", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}