Package 63323-238-61

Brand: cefazolin

Generic: cefazolin sodium
NDC Package

Package Facts

Identity

Package NDC 63323-238-61
Digits Only 6332323861
Product NDC 63323-238
Product ID 63323-238_9684b8e0-7438-41d9-89e1-b217b5568360
Description

10 VIAL in 1 CARTON (63323-238-61) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-238-01)

Marketing

Marketing Status
Marketed Since 2011-06-14
Brand cefazolin
Generic cefazolin sodium
Sample Package No

Linked Drug Pages (1)

Cefazolin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "9684b8e0-7438-41d9-89e1-b217b5568360", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["313920"], "spl_set_id": ["47a8928f-708d-418a-829b-36eded96bac0"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (63323-238-61)  / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-238-01)", "package_ndc": "63323-238-61", "marketing_start_date": "20110614"}], "brand_name": "Cefazolin", "product_id": "63323-238_9684b8e0-7438-41d9-89e1-b217b5568360", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "63323-238", "generic_name": "Cefazolin Sodium", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "10 g/1"}], "application_number": "ANDA065306", "marketing_category": "ANDA", "marketing_start_date": "20110614", "listing_expiration_date": "20261231"}