Package 76420-649-06

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 76420-649-06
Digits Only 7642064906
Product NDC 76420-649
Description

6 TABLET, FILM COATED in 1 BOTTLE (76420-649-06)

Marketing

Marketing Status
Marketed Since 2023-12-31
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": "0dc7bda4-7a99-9041-e063-6294a90a5157", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["b77b347d-d357-4bdf-b985-49d9a1dd634c"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (76420-649-06)", "package_ndc": "76420-649-06", "marketing_start_date": "20231231"}], "brand_name": "Azithromycin", "product_id": "76420-649_0dc7bda4-7a99-9041-e063-6294a90a5157", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "76420-649", "generic_name": "Azithromycin", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA210000", "marketing_category": "ANDA", "marketing_start_date": "20220411", "listing_expiration_date": "20261231"}