Package 69452-173-13

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 69452-173-13
Digits Only 6945217313
Product NDC 69452-173
Product ID 69452-173_0d48a6b6-8e7f-a3ae-e063-6394a90ada0c
Description

30 TABLET, FILM COATED in 1 BOTTLE (69452-173-13)

Marketing

Marketing Status
Marketed Since 2018-12-26
Brand azithromycin
Generic azithromycin
Sample Package No

Linked Drug Pages (1)

Azithromycin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0d48a6b6-8e7f-a3ae-e063-6394a90ada0c", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["204844"], "spl_set_id": ["a2754618-3df1-4b89-aa09-fdff4b71b7e4"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (69452-173-13)", "package_ndc": "69452-173-13", "marketing_start_date": "20181226"}], "brand_name": "Azithromycin", "product_id": "69452-173_0d48a6b6-8e7f-a3ae-e063-6394a90ada0c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "69452-173", "generic_name": "Azithromycin", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "600 mg/1"}], "application_number": "ANDA209999", "marketing_category": "ANDA", "marketing_start_date": "20181226", "listing_expiration_date": "20261231"}