Package 63323-342-25

Brand: cefoxitin

Generic: cefoxitin sodium
NDC Package

Package Facts

Identity

Package NDC 63323-342-25
Digits Only 6332334225
Product NDC 63323-342
Product ID 63323-342_9f457501-b963-49c0-89a3-4228eb493895
Description

25 VIAL in 1 CARTON (63323-342-25) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-342-01)

Marketing

Marketing Status
Marketed Since 2011-07-06
Brand cefoxitin
Generic cefoxitin sodium
Sample Package No

Linked Drug Pages (1)

Cefoxitin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "9f457501-b963-49c0-89a3-4228eb493895", "openfda": {"upc": ["0363323342012", "0363323341015"], "unii": ["Q68050H03T"], "rxcui": ["1665102", "1665107"], "spl_set_id": ["d02170ff-65aa-48b8-a922-94271c46ffa7"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (63323-342-25)  / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-342-01)", "package_ndc": "63323-342-25", "marketing_start_date": "20110706"}], "brand_name": "Cefoxitin", "product_id": "63323-342_9f457501-b963-49c0-89a3-4228eb493895", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "63323-342", "generic_name": "Cefoxitin Sodium", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefoxitin", "active_ingredients": [{"name": "CEFOXITIN SODIUM", "strength": "2 g/1"}], "application_number": "ANDA065414", "marketing_category": "ANDA", "marketing_start_date": "20110706", "listing_expiration_date": "20261231"}