Package 70518-4356-0

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 70518-4356-0
Digits Only 7051843560
Product NDC 70518-4356
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4356-0)

Marketing

Marketing Status
Marketed Since 2025-06-13
Brand azithromycin
Generic azithromycin
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40313c7e-999d-e27b-e063-6394a90ac8c7", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460"], "spl_set_id": ["da399401-1ee6-422a-be46-0bba6b264b2f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4356-0)", "package_ndc": "70518-4356-0", "marketing_start_date": "20250613"}], "brand_name": "azithromycin", "product_id": "70518-4356_40313c7e-999d-e27b-e063-6394a90ac8c7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70518-4356", "generic_name": "azithromycin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA065398", "marketing_category": "ANDA", "marketing_start_date": "20250613", "listing_expiration_date": "20261231"}