Package 16714-398-01

Brand: cefprozil

Generic: cefprozil
NDC Package

Package Facts

Identity

Package NDC 16714-398-01
Digits Only 1671439801
Product NDC 16714-398
Product ID 16714-398_1fef82c2-7104-4649-bf85-6d7bef37262e
Description

100 TABLET, FILM COATED in 1 BOTTLE (16714-398-01)

Marketing

Marketing Status
Marketed Since 2007-05-24
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": "1fef82c2-7104-4649-bf85-6d7bef37262e", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["4W0459ZA4V"], "rxcui": ["197452", "197453"], "spl_set_id": ["6133611e-19c1-4df2-8c23-8573aaf63020"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16714-398-01)", "package_ndc": "16714-398-01", "marketing_start_date": "20070524"}], "brand_name": "Cefprozil", "product_id": "16714-398_1fef82c2-7104-4649-bf85-6d7bef37262e", "dosage_form": "TABLET, FILM COATED", "product_ndc": "16714-398", "generic_name": "Cefprozil", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefprozil", "active_ingredients": [{"name": "CEFPROZIL", "strength": "250 mg/1"}], "application_number": "ANDA065340", "marketing_category": "ANDA", "marketing_start_date": "20070524", "listing_expiration_date": "20261231"}