ceftriaxone sodium

Generic: ceftriaxone sodium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ceftriaxone sodium
Generic Name ceftriaxone sodium
Labeler a-s medication solutions
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ceftriaxone sodium 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3838
Product ID 50090-3838_f3d65432-050d-4e4f-8cb7-2d20d230a350
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203702
Listing Expiration 2026-12-31
Marketing Start 2017-06-30

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500903838
Hyphenated Format 50090-3838

Supplemental Identifiers

RxCUI
1665005
UNII
023Z5BR09K

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
  • 1 VIAL, SINGLE-USE in 1 CARTON (50090-3838-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
source: ndc

Packages (1)

50090-3838-0 1 VIAL, SINGLE-USE in 1 CARTON (50090-3838-0) / 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": "f3d65432-050d-4e4f-8cb7-2d20d230a350", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665005"], "spl_set_id": ["53415af6-4072-4339-83e2-d870ae02a0e2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (50090-3838-0)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "50090-3838-0", "marketing_start_date": "20181115"}], "brand_name": "Ceftriaxone Sodium", "product_id": "50090-3838_f3d65432-050d-4e4f-8cb7-2d20d230a350", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "50090-3838", "generic_name": "Ceftriaxone Sodium", "labeler_name": "A-S Medication Solutions", "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": "20170630", "listing_expiration_date": "20261231"}