Package 50090-1710-0

Brand: cefprozil

Generic: cefprozil
NDC Package

Package Facts

Identity

Package NDC 50090-1710-0
Digits Only 5009017100
Product NDC 50090-1710
Product ID 50090-1710_ff9d76a8-9edd-4344-85dc-ee245e26d376
Description

20 TABLET, FILM COATED in 1 BOTTLE (50090-1710-0)

Marketing

Marketing Status
Marketed Since 2015-02-25
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": "ff9d76a8-9edd-4344-85dc-ee245e26d376", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["4W0459ZA4V"], "rxcui": ["197453"], "spl_set_id": ["d5d28d57-1f3c-4c80-ad78-0f67635f5428"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-1710-0)", "package_ndc": "50090-1710-0", "marketing_start_date": "20150225"}], "brand_name": "Cefprozil", "product_id": "50090-1710_ff9d76a8-9edd-4344-85dc-ee245e26d376", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50090-1710", "generic_name": "Cefprozil", "labeler_name": "A-S Medication Solutions", "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"}