Package 50111-789-10

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 50111-789-10
Digits Only 5011178910
Product NDC 50111-789
Product ID 50111-789_d6a6e6e8-3842-49a7-883b-82aa0916f3c7
Description

30 TABLET, FILM COATED in 1 BOTTLE (50111-789-10)

Marketing

Marketing Status
Marketed Since 2005-12-01
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": "d6a6e6e8-3842-49a7-883b-82aa0916f3c7", "openfda": {"unii": ["JTE4MNN1MD"], "rxcui": ["204844"], "spl_set_id": ["ac549022-4d7f-4c9f-9244-1a2df9a27276"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50111-789-10)", "package_ndc": "50111-789-10", "marketing_start_date": "20051201"}], "brand_name": "Azithromycin", "product_id": "50111-789_d6a6e6e8-3842-49a7-883b-82aa0916f3c7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "50111-789", "generic_name": "Azithromycin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN MONOHYDRATE", "strength": "600 mg/1"}], "application_number": "ANDA065218", "marketing_category": "ANDA", "marketing_start_date": "20051201", "listing_expiration_date": "20261231"}