Package 76420-589-03

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 76420-589-03
Digits Only 7642058903
Product NDC 76420-589
Description

3 TABLET, FILM COATED in 1 BLISTER PACK (76420-589-03)

Marketing

Marketing Status
Marketed Since 2023-09-01
Brand azithromycin
Generic azithromycin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "04472220-f8c1-1f1a-e063-6294a90a2bb2", "openfda": {"unii": ["JTE4MNN1MD"], "rxcui": ["248656", "308460", "749780", "749783"], "spl_set_id": ["9c44af6d-8a9a-cb4c-e053-2a95a90afdac"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BLISTER PACK (76420-589-03)", "package_ndc": "76420-589-03", "marketing_start_date": "20230901"}], "brand_name": "Azithromycin", "product_id": "76420-589_04472220-f8c1-1f1a-e063-6294a90a2bb2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "76420-589", "generic_name": "Azithromycin", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN MONOHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA065223", "marketing_category": "ANDA", "marketing_start_date": "20060106", "listing_expiration_date": "20261231"}