Package 68788-8773-3

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 68788-8773-3
Digits Only 6878887733
Product NDC 68788-8773
Product ID 68788-8773_5d400ebb-9edc-4753-9764-8d3aa9aeba41
Description

3 TABLET, FILM COATED in 1 BOTTLE (68788-8773-3)

Marketing

Marketing Status
Marketed Since 2024-11-20
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": "5d400ebb-9edc-4753-9764-8d3aa9aeba41", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["3b90572c-cc24-49f0-baaf-09022a2f9a00"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (68788-8773-3)", "package_ndc": "68788-8773-3", "marketing_start_date": "20241120"}, {"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (68788-8773-4)", "package_ndc": "68788-8773-4", "marketing_start_date": "20241120"}], "brand_name": "Azithromycin Dihydrate", "product_id": "68788-8773_5d400ebb-9edc-4753-9764-8d3aa9aeba41", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68788-8773", "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": "20241120", "listing_expiration_date": "20271231"}