Package 68071-4812-2

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 68071-4812-2
Digits Only 6807148122
Product NDC 68071-4812
Description

2 TABLET, FILM COATED in 1 BOTTLE (68071-4812-2)

Marketing

Marketing Status
Marketed Since 2025-01-31
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": "2d0644a1-e698-e6a7-e063-6394a90a3623", "openfda": {"upc": ["0368071481228"], "unii": ["5FD1131I7S"], "rxcui": ["308460"], "spl_set_id": ["a9cdb5ae-2aeb-c598-e053-2a95a90a8062"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (68071-4812-2)", "package_ndc": "68071-4812-2", "marketing_start_date": "20250131"}], "brand_name": "Azithromycin", "product_id": "68071-4812_2d0644a1-e698-e6a7-e063-6394a90a3623", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68071-4812", "generic_name": "Azithromycin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA207370", "marketing_category": "ANDA", "marketing_start_date": "20180705", "listing_expiration_date": "20261231"}