Package 71205-674-03

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 71205-674-03
Digits Only 7120567403
Product NDC 71205-674
Description

1 DOSE PACK in 1 CARTON (71205-674-03) / 3 TABLET, FILM COATED in 1 DOSE PACK

Marketing

Marketing Status
Marketed Since 2022-07-07
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": "69477c94-fdae-4d10-b4e0-2f3c566f2eba", "openfda": {"upc": ["0371205674038"], "unii": ["5FD1131I7S"], "rxcui": ["248656", "749780"], "spl_set_id": ["90605f94-93e1-43d1-8be7-830e816ac84f"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 DOSE PACK in 1 CARTON (71205-674-03)  / 3 TABLET, FILM COATED in 1 DOSE PACK", "package_ndc": "71205-674-03", "marketing_start_date": "20220707"}], "brand_name": "Azithromycin", "product_id": "71205-674_69477c94-fdae-4d10-b4e0-2f3c566f2eba", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "71205-674", "generic_name": "Azithromycin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA065212", "marketing_category": "ANDA", "marketing_start_date": "20051114", "listing_expiration_date": "20261231"}