cefepime
Generic: cefepime hydrochloride
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
cefepime
Generic Name
cefepime hydrochloride
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
cefepime hydrochloride 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
25021-121
Product ID
25021-121_a980a9e1-16f8-41c8-a8e4-31101948966c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065441
Listing Expiration
2026-12-31
Marketing Start
2008-05-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021121
Hyphenated Format
25021-121
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
ANDA065441 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 10 VIAL in 1 CARTON (25021-121-20) / 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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "a980a9e1-16f8-41c8-a8e4-31101948966c", "openfda": {"unii": ["I8X1O0607P"], "rxcui": ["1665088", "1665093"], "spl_set_id": ["de477f37-40f6-4295-ae72-a2ee36a8922e"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-121-20) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "25021-121-20", "marketing_start_date": "20080501"}], "brand_name": "cefepime", "product_id": "25021-121_a980a9e1-16f8-41c8-a8e4-31101948966c", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "25021-121", "generic_name": "cefepime hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "cefepime", "active_ingredients": [{"name": "CEFEPIME HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "ANDA065441", "marketing_category": "ANDA", "marketing_start_date": "20080501", "listing_expiration_date": "20261231"}