Package 71093-175-05

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 71093-175-05
Digits Only 7109317505
Product NDC 71093-175
Description

500 TABLET, FILM COATED in 1 BOTTLE (71093-175-05)

Marketing

Marketing Status
Marketed Since 2023-09-30
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": "77a7e874-29c3-449c-92b3-448023e67197", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["fb2f83a2-507b-4cf3-81ea-d10c46c0f8ea"], "manufacturer_name": ["ACI Healthcare USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71093-175-01)", "package_ndc": "71093-175-01", "marketing_start_date": "20230930"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71093-175-05)", "package_ndc": "71093-175-05", "marketing_start_date": "20230930"}], "brand_name": "Azithromycin Dihydrate", "product_id": "71093-175_77a7e874-29c3-449c-92b3-448023e67197", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "71093-175", "generic_name": "Azithromycin Dihydrate", "labeler_name": "ACI Healthcare USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA215773", "marketing_category": "ANDA", "marketing_start_date": "20230730", "listing_expiration_date": "20261231"}