Package 85766-008-06

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 85766-008-06
Digits Only 8576600806
Product NDC 85766-008
Description

6 DOSE PACK in 1 CARTON (85766-008-06) / 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": "49eeafc2-f6d5-2cfd-e063-6394a90a7af6", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["60ec2020-148b-4a2a-96f2-dd09c590ecbb"], "manufacturer_name": ["Sportpharm LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "6 DOSE PACK in 1 CARTON (85766-008-06)  / 1 TABLET, FILM COATED in 1 DOSE PACK", "package_ndc": "85766-008-06", "marketing_start_date": "20250618"}], "brand_name": "Azithromycin", "product_id": "85766-008_49eeafc2-f6d5-2cfd-e063-6394a90a7af6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "85766-008", "generic_name": "Azithromycin", "labeler_name": "Sportpharm LLC", "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": "20271231"}