Package 82804-214-06

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 82804-214-06
Digits Only 8280421406
Product NDC 82804-214
Product ID 82804-214_25bc2e78-9d0d-41c6-a55e-a267d4457967
Description

6 TABLET, FILM COATED in 1 BLISTER PACK (82804-214-06)

Marketing

Marketing Status
Marketed Since 2025-04-07
Brand azithromycin
Generic azithromycin
Sample Package No

Linked Drug Pages (1)

azithromycin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "25bc2e78-9d0d-41c6-a55e-a267d4457967", "openfda": {"upc": ["0382804214068"], "unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["25bc2e78-9d0d-41c6-a55e-a267d4457967"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BLISTER PACK (82804-214-06)", "package_ndc": "82804-214-06", "marketing_start_date": "20250407"}], "brand_name": "azithromycin", "product_id": "82804-214_25bc2e78-9d0d-41c6-a55e-a267d4457967", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "82804-214", "generic_name": "azithromycin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA065398", "marketing_category": "ANDA", "marketing_start_date": "20221117", "listing_expiration_date": "20261231"}