Package 68788-8311-3

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 68788-8311-3
Digits Only 6878883113
Product NDC 68788-8311
Product ID 68788-8311_45da1013-76ad-4087-b408-6526cd79f235
Description

1 BLISTER PACK in 1 CARTON (68788-8311-3) / 3 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-12-20
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": "45da1013-76ad-4087-b408-6526cd79f235", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "749780"], "spl_set_id": ["4e3ca491-2729-4250-8475-f2c9be6ba86e"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (68788-8311-3)  / 3 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "68788-8311-3", "marketing_start_date": "20221220"}], "brand_name": "Azithromycin Dihydrate", "product_id": "68788-8311_45da1013-76ad-4087-b408-6526cd79f235", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68788-8311", "generic_name": "Azithromycin Dihydrate", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20221220", "listing_expiration_date": "20261231"}