cefepime
Generic: cefepime hydrochloride
Labeler: qilu pharmaceutical co., ltd.Drug Facts
Product Profile
Brand Name
cefepime
Generic Name
cefepime hydrochloride
Labeler
qilu pharmaceutical co., ltd.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cefepime hydrochloride 2 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
67184-1004
Product ID
67184-1004_34afba66-733f-4403-83d1-1b67b8a6633b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203704
Listing Expiration
2026-12-31
Marketing Start
2016-02-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
671841004
Hyphenated Format
67184-1004
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
cefepime (source: ndc)
Generic Name
cefepime hydrochloride (source: ndc)
Application Number
ANDA203704 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 g/1
Packaging
- 10 VIAL in 1 CARTON (67184-1004-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Packages (1)
Ingredients (1)
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"}