Package 70518-3508-0
Brand: azithromycin
Generic: azithromycinPackage Facts
Identity
Package NDC
70518-3508-0
Digits Only
7051835080
Product NDC
70518-3508
Description
2 POUCH in 1 BOX (70518-3508-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3508-1)
Marketing
Marketing Status
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": "3aafb185-288b-80dc-e063-6294a90a3772", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["12e39d3d-de16-4735-8897-cbf82148a3f5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "2 POUCH in 1 BOX (70518-3508-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3508-1)", "package_ndc": "70518-3508-0", "marketing_start_date": "20220905"}], "brand_name": "Azithromycin", "product_id": "70518-3508_3aafb185-288b-80dc-e063-6294a90a3772", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70518-3508", "generic_name": "Azithromycin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA207398", "marketing_category": "ANDA", "marketing_start_date": "20220905", "listing_expiration_date": "20261231"}