Package 70518-4202-0

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 70518-4202-0
Digits Only 7051842020
Product NDC 70518-4202
Product ID 70518-4202_3ff532ea-01f0-307a-e063-6294a90a2fb7
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4202-0)

Marketing

Marketing Status
Marketed Since 2024-10-02
Brand azithromycin dihydrate
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (1)

Azithromycin Dihydrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ff532ea-01f0-307a-e063-6294a90a2fb7", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["204844"], "spl_set_id": ["0d5129e4-8b94-4a4d-baa9-be0d6b32d714"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4202-0)", "package_ndc": "70518-4202-0", "marketing_start_date": "20241002"}], "brand_name": "Azithromycin Dihydrate", "product_id": "70518-4202_3ff532ea-01f0-307a-e063-6294a90a2fb7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70518-4202", "generic_name": "Azithromycin dihydrate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "600 mg/1"}], "application_number": "ANDA207566", "marketing_category": "ANDA", "marketing_start_date": "20241002", "listing_expiration_date": "20261231"}