Package 68180-404-01

Brand: cefprozil

Generic: cefprozil
NDC Package

Package Facts

Identity

Package NDC 68180-404-01
Digits Only 6818040401
Product NDC 68180-404
Product ID 68180-404_b5bc3f77-ca01-4c3f-b8b6-591a3d8f73f4
Description

50 TABLET in 1 BOTTLE (68180-404-01)

Marketing

Marketing Status
Marketed Since 2005-12-01
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": "b5bc3f77-ca01-4c3f-b8b6-591a3d8f73f4", "openfda": {"nui": ["N0000175488", "M0003827"], "unii": ["4W0459ZA4V"], "rxcui": ["197452", "197453"], "spl_set_id": ["14527f4a-ce99-449d-a5a5-9edd7fb28dee"], "pharm_class_cs": ["Cephalosporins [CS]"], "pharm_class_epc": ["Cephalosporin Antibacterial [EPC]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (68180-404-01)", "package_ndc": "68180-404-01", "marketing_start_date": "20051201"}], "brand_name": "CEFPROZIL", "product_id": "68180-404_b5bc3f77-ca01-4c3f-b8b6-591a3d8f73f4", "dosage_form": "TABLET", "product_ndc": "68180-404", "generic_name": "CEFPROZIL", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFPROZIL", "active_ingredients": [{"name": "CEFPROZIL", "strength": "500 mg/1"}], "application_number": "ANDA065276", "marketing_category": "ANDA", "marketing_start_date": "20051201", "listing_expiration_date": "20261231"}