ceftriaxone sodium

Generic: ceftriaxone sodium

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ceftriaxone sodium
Generic Name ceftriaxone sodium
Labeler remedyrepack inc.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ceftriaxone sodium 1 g/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2499
Product ID 70518-2499_4a2c61de-94ed-eb0b-e063-6294a90a0e2a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065169
Listing Expiration 2027-12-31
Marketing Start 2019-12-19

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182499
Hyphenated Format 70518-2499

Supplemental Identifiers

RxCUI
1665021
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
  • 1 g/1
source: ndc
Packaging
  • 10 VIAL, SINGLE-USE in 1 CARTON (70518-2499-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (70518-2499-1)
source: ndc

Packages (1)

Ingredients (1)

ceftriaxone sodium (1 g/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4a2c61de-94ed-eb0b-e063-6294a90a0e2a", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665021"], "spl_set_id": ["9c801096-ca61-4b29-a1e1-5f7e7813b191"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (70518-2499-0)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (70518-2499-1)", "package_ndc": "70518-2499-0", "marketing_start_date": "20191219"}], "brand_name": "Ceftriaxone Sodium", "product_id": "70518-2499_4a2c61de-94ed-eb0b-e063-6294a90a0e2a", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "70518-2499", "generic_name": "Ceftriaxone Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065169", "marketing_category": "ANDA", "marketing_start_date": "20191219", "listing_expiration_date": "20271231"}