Package 65862-069-01

Brand: cefprozil

Generic: cefprozil
NDC Package

Package Facts

Identity

Package NDC 65862-069-01
Digits Only 6586206901
Product NDC 65862-069
Description

100 TABLET, FILM COATED in 1 BOTTLE (65862-069-01)

Marketing

Marketing Status
Marketed Since 2007-05-24
Brand cefprozil
Generic cefprozil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6397ff45-3c37-40c3-a924-d036bb896b3b", "openfda": {"nui": ["N0000175488", "M0003827"], "upc": ["0365862069016"], "unii": ["4W0459ZA4V"], "rxcui": ["197452", "197453"], "spl_set_id": ["b9111a81-07c4-4458-b994-a4ad504986d8"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-069-01)", "package_ndc": "65862-069-01", "marketing_start_date": "20070524"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-069-05)", "package_ndc": "65862-069-05", "marketing_start_date": "20070524"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-069-30)", "package_ndc": "65862-069-30", "marketing_start_date": "20070524"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (65862-069-50)", "package_ndc": "65862-069-50", "marketing_start_date": "20070524"}], "brand_name": "Cefprozil", "product_id": "65862-069_6397ff45-3c37-40c3-a924-d036bb896b3b", "dosage_form": "TABLET, FILM COATED", "product_ndc": "65862-069", "generic_name": "Cefprozil", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefprozil", "active_ingredients": [{"name": "CEFPROZIL", "strength": "500 mg/1"}], "application_number": "ANDA065340", "marketing_category": "ANDA", "marketing_start_date": "20070524", "listing_expiration_date": "20261231"}