ceftriaxone sodium

Generic: ceftriaxone sodium

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

Drug Facts

Product Profile

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

ceftriaxone sodium 500 mg/1

Manufacturer
Qilu Pharmaceutical Co., Ltd.

Identifiers & Regulatory

Product NDC 67184-1006
Product ID 67184-1006_49f990ff-ec42-da5c-e063-6294a90aee7d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203702
Listing Expiration 2027-12-31
Marketing Start 2016-06-29

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 671841006
Hyphenated Format 67184-1006

Supplemental Identifiers

RxCUI
309092 1665005 1665021 1665046
UPC
0367184100514 0367184100712 0367184100613
UNII
023Z5BR09K

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 ceftriaxone sodium (source: ndc)
Generic Name ceftriaxone sodium (source: ndc)
Application Number ANDA203702 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 10 VIAL, SINGLE-USE in 1 CARTON (67184-1006-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
  • 1 VIAL, SINGLE-USE in 1 CARTON (67184-1006-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
source: ndc

Packages (2)

67184-1006-1 10 VIAL, SINGLE-USE in 1 CARTON (67184-1006-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE 67184-1006-2 1 VIAL, SINGLE-USE in 1 CARTON (67184-1006-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

Ingredients (1)

ceftriaxone sodium (500 mg/1)

Linked Drug Pages (1)

Ceftriaxone Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "49f990ff-ec42-da5c-e063-6294a90aee7d", "openfda": {"upc": ["0367184100514", "0367184100712", "0367184100613"], "unii": ["023Z5BR09K"], "rxcui": ["309092", "1665005", "1665021", "1665046"], "spl_set_id": ["4cdf0743-c62b-4969-b9c9-4c6400644f6c"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (67184-1006-1)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "67184-1006-1", "marketing_start_date": "20160629"}, {"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (67184-1006-2)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "67184-1006-2", "marketing_start_date": "20160629"}], "brand_name": "Ceftriaxone Sodium", "product_id": "67184-1006_49f990ff-ec42-da5c-e063-6294a90aee7d", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67184-1006", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA203702", "marketing_category": "ANDA", "marketing_start_date": "20160629", "listing_expiration_date": "20271231"}