cefazolin
Generic: cefazolin
Labeler: qilu pharmaceutical co., ltd.Drug Facts
Product Profile
Brand Name
cefazolin
Generic Name
cefazolin
Labeler
qilu pharmaceutical co., ltd.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cefazolin sodium 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
67184-1001
Product ID
67184-1001_0cc53b72-80e0-4a82-e063-6394a90a7fdf
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203661
Listing Expiration
2026-12-31
Marketing Start
2015-12-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
671841001
Hyphenated Format
67184-1001
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
cefazolin (source: ndc)
Generic Name
cefazolin (source: ndc)
Application Number
ANDA203661 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 25 VIAL in 1 CARTON (67184-1001-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0cc53b72-80e0-4a82-e063-6394a90a7fdf", "openfda": {"unii": ["P380M0454Z"], "rxcui": ["1665050", "1665060"], "spl_set_id": ["e8bd9e95-8af5-416b-b58c-e1dbe3d052ac"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (67184-1001-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "67184-1001-2", "marketing_start_date": "20151228"}], "brand_name": "Cefazolin", "product_id": "67184-1001_0cc53b72-80e0-4a82-e063-6394a90a7fdf", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67184-1001", "generic_name": "Cefazolin", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "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": "20151228", "listing_expiration_date": "20261231"}