Package 63323-341-29

Brand: cefoxitin

Generic: cefoxitin sodium
NDC Package

Package Facts

Identity

Package NDC 63323-341-29
Digits Only 6332334129
Product NDC 63323-341
Product ID 63323-341_0fffe10d-e5bc-4a0c-ae5b-bbf4095990ba
Description

25 VIAL in 1 CARTON (63323-341-29) / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-341-41)

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": "0fffe10d-e5bc-4a0c-ae5b-bbf4095990ba", "openfda": {"upc": ["0363323341411", "0363323342418"], "unii": ["Q68050H03T"], "rxcui": ["1665102", "1665107"], "spl_set_id": ["2a9d1e7b-96ee-4e6c-a1e8-47b76b924422"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (63323-341-29)  / 1 POWDER, FOR SOLUTION in 1 VIAL (63323-341-41)", "package_ndc": "63323-341-29", "marketing_start_date": "20110706"}], "brand_name": "Cefoxitin", "product_id": "63323-341_0fffe10d-e5bc-4a0c-ae5b-bbf4095990ba", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "63323-341", "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": "1 g/1"}], "application_number": "ANDA065414", "marketing_category": "ANDA", "marketing_start_date": "20110706", "listing_expiration_date": "20261231"}