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 2 g/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-710
Product ID 71205-710_a25ab5ea-c46d-4562-8f7e-0ccffc2ab069
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065169
Listing Expiration 2026-12-31
Marketing Start 2005-05-09

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205710
Hyphenated Format 71205-710

Supplemental Identifiers

RxCUI
1665046
UPC
0371205710019
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 ANDA065169 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 g/1
source: ndc
Packaging
  • 1 VIAL, SINGLE-USE in 1 CARTON (71205-710-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
source: ndc

Packages (1)

71205-710-01 1 VIAL, SINGLE-USE in 1 CARTON (71205-710-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

Ingredients (1)

ceftriaxone sodium (2 g/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": "a25ab5ea-c46d-4562-8f7e-0ccffc2ab069", "openfda": {"upc": ["0371205710019"], "unii": ["023Z5BR09K"], "rxcui": ["1665046"], "spl_set_id": ["a25ab5ea-c46d-4562-8f7e-0ccffc2ab069"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (71205-710-01)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "71205-710-01", "marketing_start_date": "20221031"}], "brand_name": "Ceftriaxone Sodium", "product_id": "71205-710_a25ab5ea-c46d-4562-8f7e-0ccffc2ab069", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "71205-710", "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": "2 g/1"}], "application_number": "ANDA065169", "marketing_category": "ANDA", "marketing_start_date": "20050509", "listing_expiration_date": "20261231"}