Package 0404-9835-99

Brand: cefazolin

Generic: cefazolin
NDC Package

Package Facts

Identity

Package NDC 0404-9835-99
Digits Only 0404983599
Product NDC 0404-9835
Description

1 VIAL in 1 BAG (0404-9835-99) / 2.2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-01-09
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": "a5e569a1-da41-44da-a31a-3c9d2c0b61c2", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665052"], "spl_set_id": ["922fb1a1-ad4c-4a12-8d5d-00fe13af18e8"], "manufacturer_name": ["Henry Schein Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9835-99)  / 2.2 mL in 1 VIAL", "package_ndc": "0404-9835-99", "marketing_start_date": "20220109"}], "brand_name": "CEFAZOLIN", "product_id": "0404-9835_a5e569a1-da41-44da-a31a-3c9d2c0b61c2", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0404-9835", "generic_name": "cefazolin", "labeler_name": "Henry Schein Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CEFAZOLIN", "active_ingredients": [{"name": "CEFAZOLIN SODIUM", "strength": "225 mg/mL"}], "application_number": "ANDA065047", "marketing_category": "ANDA", "marketing_start_date": "20220109", "listing_expiration_date": "20261231"}