Package 67184-1004-1

Brand: cefepime

Generic: cefepime hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67184-1004-1
Digits Only 6718410041
Product NDC 67184-1004
Description

10 VIAL in 1 CARTON (67184-1004-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2016-02-01
Brand cefepime
Generic cefepime hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "34afba66-733f-4403-83d1-1b67b8a6633b", "openfda": {"unii": ["I8X1O0607P"], "rxcui": ["1665088", "1665093", "1665097"], "spl_set_id": ["80b4c811-4a71-47fb-8565-85ce9d0f782c"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (67184-1004-1)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "67184-1004-1", "marketing_start_date": "20160201"}], "brand_name": "Cefepime", "product_id": "67184-1004_34afba66-733f-4403-83d1-1b67b8a6633b", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67184-1004", "generic_name": "CEFEPIME HYDROCHLORIDE", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefepime", "active_ingredients": [{"name": "CEFEPIME HYDROCHLORIDE", "strength": "2 g/1"}], "application_number": "ANDA203704", "marketing_category": "ANDA", "marketing_start_date": "20160201", "listing_expiration_date": "20261231"}