Package 67046-1502-3

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 67046-1502-3
Digits Only 6704615023
Product NDC 67046-1502
Product ID 67046-1502_2cc99fae-a6c4-8893-e063-6394a90aa3ef
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1502-3)

Marketing

Marketing Status
Marketed Since 2025-01-28
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": "2cc99fae-a6c4-8893-e063-6394a90aa3ef", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460"], "spl_set_id": ["2cc99fae-a72c-8893-e063-6394a90aa3ef"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1502-3)", "package_ndc": "67046-1502-3", "marketing_start_date": "20250128"}], "brand_name": "Azithromycin Dihydrate", "product_id": "67046-1502_2cc99fae-a6c4-8893-e063-6394a90aa3ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "67046-1502", "generic_name": "Azithromycin Dihydrate", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA208250", "marketing_category": "ANDA", "marketing_start_date": "20250128", "listing_expiration_date": "20261231"}