cefepime

Generic: cefepime

Labeler: apotex corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefepime
Generic Name cefepime
Labeler apotex corp.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

cefepime hydrochloride 1 g/1

Manufacturer
Apotex Corp.

Identifiers & Regulatory

Product NDC 60505-6146
Product ID 60505-6146_e1dbb0ac-a9df-41c4-acb2-3e3f5732f7ef
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203704
Listing Expiration 2026-12-31
Marketing Start 2017-03-30

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 605056146
Hyphenated Format 60505-6146

Supplemental Identifiers

RxCUI
1665088 1665093
UPC
0360505614608 0360505614707
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 (source: ndc)
Application Number ANDA203704 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (60505-6146-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6146-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (2)

60505-6146-0 1 VIAL, SINGLE-DOSE in 1 CARTON (60505-6146-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE 60505-6146-4 10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6146-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE

Ingredients (1)

cefepime hydrochloride (1 g/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": "e1dbb0ac-a9df-41c4-acb2-3e3f5732f7ef", "openfda": {"upc": ["0360505614608", "0360505614707"], "unii": ["I8X1O0607P"], "rxcui": ["1665088", "1665093"], "spl_set_id": ["dd641c7f-b857-48ff-bd9d-747e0c3cc89f"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (60505-6146-0)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "60505-6146-0", "marketing_start_date": "20170330"}, {"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6146-4)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "60505-6146-4", "marketing_start_date": "20170330"}], "brand_name": "Cefepime", "product_id": "60505-6146_e1dbb0ac-a9df-41c4-acb2-3e3f5732f7ef", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "60505-6146", "generic_name": "Cefepime", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefepime", "active_ingredients": [{"name": "CEFEPIME HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA203704", "marketing_category": "ANDA", "marketing_start_date": "20170330", "listing_expiration_date": "20261231"}