Package 67046-1607-3

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 67046-1607-3
Digits Only 6704616073
Product NDC 67046-1607
Product ID 67046-1607_4196de9a-0c36-7cfe-e063-6394a90a409a
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1607-3)

Marketing

Marketing Status
Marketed Since 2025-10-20
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": "4196de9a-0c36-7cfe-e063-6394a90a409a", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["4196e616-bdd8-9e88-e063-6394a90ac81d"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1607-3)", "package_ndc": "67046-1607-3", "marketing_start_date": "20251020"}], "brand_name": "Azithromycin Dihydrate", "product_id": "67046-1607_4196de9a-0c36-7cfe-e063-6394a90a409a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "67046-1607", "generic_name": "Azithromycin dihydrate", "labeler_name": "Coupler LLC", "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": "20251020", "listing_expiration_date": "20261231"}