Package 71205-710-01

Brand: ceftriaxone sodium

Generic: ceftriaxone sodium
NDC Package

Package Facts

Identity

Package NDC 71205-710-01
Digits Only 7120571001
Product NDC 71205-710
Product ID 71205-710_a25ab5ea-c46d-4562-8f7e-0ccffc2ab069
Description

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

Marketing

Marketing Status
Marketed Since 2022-10-31
Brand ceftriaxone sodium
Generic ceftriaxone sodium
Sample Package No

Linked Drug Pages (1)

Ceftriaxone Sodium ndc-match (0.95)

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"}