Package 50090-4700-0

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 50090-4700-0
Digits Only 5009047000
Product NDC 50090-4700
Description

3 CARTON in 1 BOX (50090-4700-0) / 1 TABLET, FILM COATED in 1 CARTON

Marketing

Marketing Status
Marketed Since 2019-11-08
Brand azithromycin dihydrate
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fd1fcc97-fc81-4396-a789-b92409cbf4a7", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "749780"], "spl_set_id": ["0f36ba37-a742-41c1-ad2d-b890a1d49c55"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "3 CARTON in 1 BOX (50090-4700-0)  / 1 TABLET, FILM COATED in 1 CARTON", "package_ndc": "50090-4700-0", "marketing_start_date": "20191108"}], "brand_name": "Azithromycin Dihydrate", "product_id": "50090-4700_fd1fcc97-fc81-4396-a789-b92409cbf4a7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "50090-4700", "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": "20190701", "listing_expiration_date": "20261231"}