Package 50268-074-15
Brand: azithromycin dihydrate
Generic: azithromycin dihydratePackage Facts
Identity
Package NDC
50268-074-15
Digits Only
5026807415
Product NDC
50268-074
Description
50 BLISTER PACK in 1 BOX (50268-074-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-074-11)
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": "47e22fe1-c6d6-576b-e063-6394a90a98e6", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "308460"], "spl_set_id": ["b635019e-7fd4-7f9e-e053-2a95a90a388c"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-074-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-074-11)", "package_ndc": "50268-074-15", "marketing_start_date": "20210826"}], "brand_name": "Azithromycin Dihydrate", "product_id": "50268-074_47e22fe1-c6d6-576b-e063-6394a90a98e6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "50268-074", "generic_name": "Azithromycin Dihydrate", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA208250", "marketing_category": "ANDA", "marketing_start_date": "20201211", "listing_expiration_date": "20271231"}