Package 63323-236-10

Brand: cefazolin

Generic: cefazolin sodium
NDC Package

Package Facts

Identity

Package NDC 63323-236-10
Digits Only 6332323610
Product NDC 63323-236
Description

25 VIAL in 1 CARTON (63323-236-10) / 2.2 mL in 1 VIAL (63323-236-01)

Marketing

Marketing Status
Marketed Since 2011-07-15
Brand cefazolin
Generic cefazolin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "321ffc80-ee94-4a86-8c33-e966438d9fbb", "openfda": {"upc": ["0363323237011", "0363323236014"], "unii": ["P380M0454Z"], "rxcui": ["1665050", "1665052"], "spl_set_id": ["c47c8d14-1eef-40f9-9d11-f0c300b1d4be"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (63323-236-10)  / 2.2 mL in 1 VIAL (63323-236-01)", "package_ndc": "63323-236-10", "marketing_start_date": "20110715"}], "brand_name": "CEFAZOLIN", "product_id": "63323-236_321ffc80-ee94-4a86-8c33-e966438d9fbb", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "63323-236", "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": "500 mg/2.2mL"}], "application_number": "ANDA065303", "marketing_category": "ANDA", "marketing_start_date": "20110715", "listing_expiration_date": "20261231"}