Package 68071-4976-3
Brand: azithromycin
Generic: azithromycinPackage Facts
Identity
Package NDC
68071-4976-3
Digits Only
6807149763
Product NDC
68071-4976
Description
3 TABLET, FILM COATED in 1 BLISTER PACK (68071-4976-3)
Marketing
Marketing Status
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": "1b2e96de-5ed6-c9e9-e063-6394a90a472e", "openfda": {"upc": ["0368071497632"], "unii": ["5FD1131I7S"], "rxcui": ["248656", "749780"], "spl_set_id": ["8e7184e1-3c3c-cd87-e053-2a95a90a6eb6"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BLISTER PACK (68071-4976-3)", "package_ndc": "68071-4976-3", "marketing_start_date": "20190724"}], "brand_name": "Azithromycin", "product_id": "68071-4976_1b2e96de-5ed6-c9e9-e063-6394a90a472e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68071-4976", "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"}