Package 0093-4059-53

Brand: cefadroxil

Generic: cefadroxil
NDC Package

Package Facts

Identity

Package NDC 0093-4059-53
Digits Only 0093405953
Product NDC 0093-4059
Description

50 TABLET in 1 BOTTLE (0093-4059-53)

Marketing

Marketing Status
Marketed Since 2007-01-31
Brand cefadroxil
Generic cefadroxil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "980978a7-5c16-4350-add2-dd7c88ecb91b", "openfda": {"unii": ["280111G160"], "rxcui": ["309047"], "spl_set_id": ["4674a05c-fdef-4737-a4b8-e3229bdada9d"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (0093-4059-53)", "package_ndc": "0093-4059-53", "marketing_start_date": "20070131"}], "brand_name": "Cefadroxil", "product_id": "0093-4059_980978a7-5c16-4350-add2-dd7c88ecb91b", "dosage_form": "TABLET", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0093-4059", "generic_name": "Cefadroxil", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefadroxil", "active_ingredients": [{"name": "CEFADROXIL", "strength": "1000 mg/1"}], "application_number": "ANDA062774", "marketing_category": "ANDA", "marketing_start_date": "20070131", "listing_expiration_date": "20261231"}