Package 68071-5058-3

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 68071-5058-3
Digits Only 6807150583
Product NDC 68071-5058
Description

3 TABLET, FILM COATED in 1 BLISTER PACK (68071-5058-3)

Marketing

Marketing Status
Marketed Since 2019-09-13
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": "1b4318a7-a74c-c7bc-e063-6394a90aeafb", "openfda": {"upc": ["0368071505832"], "unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["9270e676-3382-6483-e053-2a95a90a556e"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BLISTER PACK (68071-5058-3)", "package_ndc": "68071-5058-3", "marketing_start_date": "20190913"}], "brand_name": "Azithromycin", "product_id": "68071-5058_1b4318a7-a74c-c7bc-e063-6394a90aeafb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68071-5058", "generic_name": "Azithromycin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA207398", "marketing_category": "ANDA", "marketing_start_date": "20180705", "listing_expiration_date": "20261231"}