ceftriaxone sodium

Generic: ceftriaxone sodium

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ceftriaxone sodium
Generic Name ceftriaxone sodium
Labeler proficient rx lp
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ceftriaxone sodium 500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-066
Product ID 82804-066_790279d4-2456-4091-abec-960b78885432
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 82804066
Hyphenated Format 82804-066

Supplemental Identifiers

RxCUI
1665005
UPC
0382804066018
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 (82804-066-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
  • 10 VIAL, SINGLE-USE in 1 CARTON (82804-066-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
source: ndc

Packages (2)

82804-066-01 1 VIAL, SINGLE-USE in 1 CARTON (82804-066-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE 82804-066-10 10 VIAL, SINGLE-USE in 1 CARTON (82804-066-10) / 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": "790279d4-2456-4091-abec-960b78885432", "openfda": {"upc": ["0382804066018"], "unii": ["023Z5BR09K"], "rxcui": ["1665005"], "spl_set_id": ["790279d4-2456-4091-abec-960b78885432"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (82804-066-01)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "82804-066-01", "marketing_start_date": "20240202"}, {"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (82804-066-10)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "82804-066-10", "marketing_start_date": "20240202"}], "brand_name": "Ceftriaxone Sodium", "product_id": "82804-066_790279d4-2456-4091-abec-960b78885432", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "82804-066", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Proficient Rx LP", "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"}