cefepime
Generic: cefepime
Labeler: apotex corp.Drug Facts
Product Profile
Brand Name
cefepime
Generic Name
cefepime
Labeler
apotex corp.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cefepime hydrochloride 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
60505-6144
Product ID
60505-6144_12c44be3-e077-4579-ad2e-868b503eadb5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203704
Listing Expiration
2026-12-31
Marketing Start
2017-11-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
605056144
Hyphenated Format
60505-6144
Supplemental Identifiers
RxCUI
UPC
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 (source: ndc)
Application Number
ANDA203704 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6144-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "12c44be3-e077-4579-ad2e-868b503eadb5", "openfda": {"upc": ["0360505614509", "0360505614400"], "unii": ["I8X1O0607P"], "rxcui": ["1665088", "1665093"], "spl_set_id": ["d63d360a-15ec-44a4-b80d-b2a5cb5759eb"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6144-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "60505-6144-4", "marketing_start_date": "20171114"}], "brand_name": "Cefepime", "product_id": "60505-6144_12c44be3-e077-4579-ad2e-868b503eadb5", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "60505-6144", "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": "20171114", "listing_expiration_date": "20261231"}