Package 72789-483-04

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 72789-483-04
Digits Only 7278948304
Product NDC 72789-483
Product ID 72789-483_47bf5b3f-0858-5c91-e063-6394a90adba4
Description

4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-483-04)

Marketing

Marketing Status
Marketed Since 2025-01-22
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": "47bf5b3f-0858-5c91-e063-6394a90adba4", "openfda": {"upc": ["0372789483047"], "unii": ["5FD1131I7S"], "rxcui": ["308460"], "spl_set_id": ["7ab854bf-eb04-42c4-a403-096b60581bb4"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-483-04)", "package_ndc": "72789-483-04", "marketing_start_date": "20250122"}], "brand_name": "Azithromycin Dihydrate", "product_id": "72789-483_47bf5b3f-0858-5c91-e063-6394a90adba4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "72789-483", "generic_name": "Azithromycin Dihydrate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20240215", "listing_expiration_date": "20271231"}