Package 71205-679-01

Brand: cefazolin

Generic: cefazolin
NDC Package

Package Facts

Identity

Package NDC 71205-679-01
Digits Only 7120567901
Product NDC 71205-679
Description

1 VIAL, SINGLE-DOSE in 1 BOX (71205-679-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-08-01
Brand cefazolin
Generic cefazolin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "d24529e3-e2b4-46d6-81ba-b7da74501792", "openfda": {"upc": ["0371205679019"], "unii": ["P380M0454Z"], "rxcui": ["1665050"], "spl_set_id": ["d24529e3-e2b4-46d6-81ba-b7da74501792"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BOX (71205-679-01)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "71205-679-01", "marketing_start_date": "20220801"}], "brand_name": "Cefazolin", "product_id": "71205-679_d24529e3-e2b4-46d6-81ba-b7da74501792", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "71205-679", "generic_name": "Cefazolin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefazolin", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "1 g/1"}], "application_number": "ANDA203661", "marketing_category": "ANDA", "marketing_start_date": "20170630", "listing_expiration_date": "20261231"}