Package 68071-2266-4

Brand: azithromycin

Generic: azithromycin
NDC Package

Package Facts

Identity

Package NDC 68071-2266-4
Digits Only 6807122664
Product NDC 68071-2266
Product ID 68071-2266_1d765adb-1f8f-1537-e063-6394a90a3ae0
Description

4 TABLET, FILM COATED in 1 BOTTLE (68071-2266-4)

Marketing

Marketing Status
Marketed Since 2020-09-24
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": "1d765adb-1f8f-1537-e063-6394a90a3ae0", "openfda": {"upc": ["0368071226645"], "unii": ["5FD1131I7S"], "rxcui": ["308460"], "spl_set_id": ["b0138503-ddc4-2e1c-e053-2995a90a0d2d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (68071-2266-4)", "package_ndc": "68071-2266-4", "marketing_start_date": "20200924"}], "brand_name": "Azithromycin", "product_id": "68071-2266_1d765adb-1f8f-1537-e063-6394a90a3ae0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68071-2266", "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": "ANDA210000", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}