Package 66288-6100-1

Brand: ceftriaxone

Generic: ceftriaxone sodium
NDC Package

Package Facts

Identity

Package NDC 66288-6100-1
Digits Only 6628861001
Product NDC 66288-6100
Description

1 INJECTION, POWDER, FOR SOLUTION in 1 BAG (66288-6100-1)

Marketing

Marketing Status
Marketed Since 2014-06-30
Brand ceftriaxone
Generic ceftriaxone sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "6aff16e3-f491-4175-a3f2-842bed6ebecb", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309090"], "spl_set_id": ["5cd2d96f-83e5-4326-ae87-d0ede4ba493a"], "manufacturer_name": ["Samson Medical Technologies, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 BAG (66288-6100-1)", "package_ndc": "66288-6100-1", "marketing_start_date": "20140630"}], "brand_name": "Ceftriaxone", "product_id": "66288-6100_6aff16e3-f491-4175-a3f2-842bed6ebecb", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "66288-6100", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Samson Medical Technologies, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "100 g/1"}], "application_number": "ANDA090057", "marketing_category": "ANDA", "marketing_start_date": "20140630", "listing_expiration_date": "20261231"}