cefazolin

Generic: cefazolin

Labeler: qilu pharmaceutical co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefazolin
Generic Name cefazolin
Labeler qilu pharmaceutical co., ltd.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

cefazolin sodium 1 g/1

Manufacturer
Qilu Pharmaceutical Co., Ltd.

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
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 671841001
Hyphenated Format 67184-1001

Supplemental Identifiers

RxCUI
1665050 1665060
UNII
P380M0454Z

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (67184-1001-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

cefazolin sodium (1 g/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"}