Package 50090-7506-0

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 50090-7506-0
Digits Only 5009075060
Product NDC 50090-7506
Description

3 CARTON in 1 BOX (50090-7506-0) / 1 TABLET, FILM COATED in 1 CARTON

Marketing

Marketing Status
Marketed Since 2025-02-17
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": "37b443e6-54a1-4c09-b097-2ea9cc785d49", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["de5b0c2b-9a7d-46e9-8169-4100442efa9b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "3 CARTON in 1 BOX (50090-7506-0)  / 1 TABLET, FILM COATED in 1 CARTON", "package_ndc": "50090-7506-0", "marketing_start_date": "20250217"}], "brand_name": "Azithromycin Dihydrate", "product_id": "50090-7506_37b443e6-54a1-4c09-b097-2ea9cc785d49", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "50090-7506", "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": "20271231"}