Package 72789-445-07

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 72789-445-07
Digits Only 7278944507
Product NDC 72789-445
Description

7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-445-07)

Marketing

Marketing Status
Marketed Since 2024-10-22
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": "47a9d9a0-55c6-0d22-e063-6394a90a1518", "openfda": {"upc": ["0372789445076"], "unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["0c926669-62b2-4ad3-8289-173c5818a9c1"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-445-02)", "package_ndc": "72789-445-02", "marketing_start_date": "20241104"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-445-07)", "package_ndc": "72789-445-07", "marketing_start_date": "20241022"}, {"sample": false, "description": "1 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-445-79)", "package_ndc": "72789-445-79", "marketing_start_date": "20241210"}], "brand_name": "Azithromycin Dihydrate", "product_id": "72789-445_47a9d9a0-55c6-0d22-e063-6394a90a1518", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "72789-445", "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": "500 mg/1"}], "application_number": "ANDA208249", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20271231"}