Package 0093-1077-01

Brand: cefprozil

Generic: cefprozil
NDC Package

Package Facts

Identity

Package NDC 0093-1077-01
Digits Only 0093107701
Product NDC 0093-1077
Product ID 0093-1077_c226712f-00c2-407f-8b40-5ed1be54dfb8
Description

100 TABLET, FILM COATED in 1 BOTTLE (0093-1077-01)

Marketing

Marketing Status
Marketed Since 2005-12-23
Brand cefprozil
Generic cefprozil
Sample Package No

Linked Drug Pages (1)

Cefprozil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c226712f-00c2-407f-8b40-5ed1be54dfb8", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["4W0459ZA4V"], "rxcui": ["197452", "197453"], "spl_set_id": ["3391de8b-7bc9-4624-a5c4-836135b39d99"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-1077-01)", "package_ndc": "0093-1077-01", "marketing_start_date": "20051223"}], "brand_name": "Cefprozil", "product_id": "0093-1077_c226712f-00c2-407f-8b40-5ed1be54dfb8", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0093-1077", "generic_name": "Cefprozil", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefprozil", "active_ingredients": [{"name": "CEFPROZIL", "strength": "250 mg/1"}], "application_number": "ANDA065208", "marketing_category": "ANDA", "marketing_start_date": "20051223", "listing_expiration_date": "20261231"}