cefepime

Generic: cefepime hydrochloride

Labeler: qilu pharmaceutical co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefepime
Generic Name cefepime hydrochloride
Labeler qilu pharmaceutical co., ltd.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

cefepime hydrochloride 500 mg/1

Manufacturer
Qilu Pharmaceutical Co., Ltd.

Identifiers & Regulatory

Product NDC 67184-1002
Product ID 67184-1002_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
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 671841002
Hyphenated Format 67184-1002

Supplemental Identifiers

RxCUI
1665088 1665093 1665097
UNII
I8X1O0607P

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (67184-1002-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

67184-1002-1 10 VIAL in 1 CARTON (67184-1002-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

Ingredients (1)

cefepime hydrochloride (500 mg/1)

Linked Drug Pages (1)

Cefepime ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "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 (67184-1002-1)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "67184-1002-1", "marketing_start_date": "20160201"}], "brand_name": "Cefepime", "product_id": "67184-1002_34afba66-733f-4403-83d1-1b67b8a6633b", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "67184-1002", "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": "500 mg/1"}], "application_number": "ANDA203704", "marketing_category": "ANDA", "marketing_start_date": "20160201", "listing_expiration_date": "20261231"}