Package 71093-174-01

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 71093-174-01
Digits Only 7109317401
Product NDC 71093-174
Product ID 71093-174_5df20b25-1932-414b-b028-210e839c1c38
Description

30 TABLET, FILM COATED in 1 BOTTLE (71093-174-01)

Marketing

Marketing Status
Marketed Since 2022-12-01
Brand azithromycin dihydrate
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (1)

Azithromycin Dihydrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5df20b25-1932-414b-b028-210e839c1c38", "openfda": {"upc": ["0371093174054"], "unii": ["5FD1131I7S"], "rxcui": ["308460"], "spl_set_id": ["39a808c4-72ac-48e4-bfb8-e5ae3429b225"], "manufacturer_name": ["ACI Healthcare USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71093-174-01)", "package_ndc": "71093-174-01", "marketing_start_date": "20221201"}], "brand_name": "Azithromycin Dihydrate", "product_id": "71093-174_5df20b25-1932-414b-b028-210e839c1c38", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "71093-174", "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": "250 mg/1"}], "application_number": "ANDA215772", "marketing_category": "ANDA", "marketing_start_date": "20221201", "listing_expiration_date": "20261231"}