Package 72789-081-04

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 72789-081-04
Digits Only 7278908104
Product NDC 72789-081
Description

4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-081-04)

Marketing

Marketing Status
Discontinued 2026-11-30
Brand azithromycin dihydrate
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31442118-2505-0be0-e063-6294a90a12d1", "openfda": {"upc": ["0372789081045"], "unii": ["5FD1131I7S"], "rxcui": ["308460"], "spl_set_id": ["e9800bbe-e8bf-4689-a8a5-dc23b5d2ee56"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-081-04)", "package_ndc": "72789-081-04", "marketing_end_date": "20261130", "marketing_start_date": "20200507"}], "brand_name": "Azithromycin Dihydrate", "product_id": "72789-081_31442118-2505-0be0-e063-6294a90a12d1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "72789-081", "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_end_date": "20261130", "marketing_start_date": "20190701"}