Package 67184-1008-1

Brand: ceftriaxone sodium

Generic: ceftriaxone sodium
NDC Package

Package Facts

Identity

Package NDC 67184-1008-1
Digits Only 6718410081
Product NDC 67184-1008
Product ID 67184-1008_49f990ff-ec42-da5c-e063-6294a90aee7d
Description

10 VIAL, SINGLE-USE in 1 CARTON (67184-1008-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2016-06-29
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": "49f990ff-ec42-da5c-e063-6294a90aee7d", "openfda": {"upc": ["0367184100514", "0367184100712", "0367184100613"], "unii": ["023Z5BR09K"], "rxcui": ["309092", "1665005", "1665021", "1665046"], "spl_set_id": ["4cdf0743-c62b-4969-b9c9-4c6400644f6c"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (67184-1008-1)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "67184-1008-1", "marketing_start_date": "20160629"}], "brand_name": "Ceftriaxone Sodium", "product_id": "67184-1008_49f990ff-ec42-da5c-e063-6294a90aee7d", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67184-1008", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "2 g/1"}], "application_number": "ANDA203702", "marketing_category": "ANDA", "marketing_start_date": "20160629", "listing_expiration_date": "20271231"}