Package 70518-3723-2
Brand: azithromycin dihydrate
Generic: azithromycin dihydratePackage Facts
Identity
Package NDC
70518-3723-2
Digits Only
7051837232
Product NDC
70518-3723
Description
2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3723-2)
Marketing
Marketing Status
Brand
azithromycin dihydrate
Generic
azithromycin dihydrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "37c3f70d-0dd3-f2ba-e063-6294a90a301a", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "749780"], "spl_set_id": ["b70fe56d-48c4-48ed-a40d-0ffcbd17b355"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3723-2)", "package_ndc": "70518-3723-2", "marketing_end_date": "20260630", "marketing_start_date": "20240219"}], "brand_name": "azithromycin dihydrate", "product_id": "70518-3723_37c3f70d-0dd3-f2ba-e063-6294a90a301a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70518-3723", "generic_name": "azithromycin dihydrate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "azithromycin dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA065399", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20230425"}