Package 76420-404-06

Brand: Azithromycin

Generic: Azithromycin
NDC Package

Package Facts

Identity

Package NDC 76420-404-06
Digits Only 7642040406
Product NDC 76420-404
Description

6 DOSE PACK in 1 CARTON (76420-404-06) / 1 TABLET, FILM COATED in 1 DOSE PACK

Marketing

Marketing Status
Marketed Since 2025-06-18
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": "37fd3847-b883-06dc-e063-6394a90ad234", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["4dc2d95d-419d-4401-8f63-68f9287198e6"], "manufacturer_name": ["ASCLEMED USA INC."]}, "finished": true, "packaging": [{"sample": false, "description": "6 DOSE PACK in 1 CARTON (76420-404-06)  / 1 TABLET, FILM COATED in 1 DOSE PACK", "package_ndc": "76420-404-06", "marketing_start_date": "20250618"}], "brand_name": "Azithromycin", "product_id": "76420-404_37fd3847-b883-06dc-e063-6394a90ad234", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "76420-404", "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": "ANDA065211", "marketing_category": "ANDA", "marketing_start_date": "20051114", "listing_expiration_date": "20261231"}