Package 63323-385-10

Brand: cefotetan

Generic: cefotetan disodium
NDC Package

Package Facts

Identity

Package NDC 63323-385-10
Digits Only 6332338510
Product NDC 63323-385
Product ID 63323-385_a30c7fcf-f9c0-4b38-bfed-fbd3b1a3e2f8
Description

10 VIAL in 1 CARTON (63323-385-10) / 10 mL in 1 VIAL (63323-385-01)

Marketing

Marketing Status
Marketed Since 2009-11-18
Brand cefotetan
Generic cefotetan disodium
Sample Package No

Linked Drug Pages (1)

Cefotetan ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "a30c7fcf-f9c0-4b38-bfed-fbd3b1a3e2f8", "openfda": {"unii": ["0GXP746VXB"], "rxcui": ["1722919", "1722921"], "spl_set_id": ["bd22c66b-8a1c-44c8-b5b6-3ab0ce5c800e"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (63323-385-10)  / 10 mL in 1 VIAL (63323-385-01)", "package_ndc": "63323-385-10", "marketing_start_date": "20091118"}], "brand_name": "Cefotetan", "product_id": "63323-385_a30c7fcf-f9c0-4b38-bfed-fbd3b1a3e2f8", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "63323-385", "generic_name": "CEFOTETAN DISODIUM", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefotetan", "active_ingredients": [{"name": "CEFOTETAN DISODIUM", "strength": "1 g/10mL"}], "application_number": "ANDA065374", "marketing_category": "ANDA", "marketing_start_date": "20091118", "listing_expiration_date": "20261231"}