Package 50090-7298-0

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 50090-7298-0
Digits Only 5009072980
Product NDC 50090-7298
Description

5 TABLET, FILM COATED in 1 BOTTLE (50090-7298-0)

Marketing

Marketing Status
Marketed Since 2024-10-14
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": "7c55988f-8092-42b4-b993-8ffb2fb0d85c", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["fcf098d5-dfd5-4a0d-81f7-6afa1a203a27"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE (50090-7298-0)", "package_ndc": "50090-7298-0", "marketing_start_date": "20241014"}, {"sample": false, "description": "1 TABLET, FILM COATED in 1 BOTTLE (50090-7298-1)", "package_ndc": "50090-7298-1", "marketing_start_date": "20241014"}], "brand_name": "Azithromycin Dihydrate", "product_id": "50090-7298_7c55988f-8092-42b4-b993-8ffb2fb0d85c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "50090-7298", "generic_name": "Azithromycin dihydrate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA208249", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}