cefepime

Generic: cefepime hydrochloride

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefepime
Generic Name cefepime hydrochloride
Labeler sagent pharmaceuticals
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

cefepime hydrochloride 1 g/1

Manufacturer
Sagent Pharmaceuticals

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
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021121
Hyphenated Format 25021-121

Supplemental Identifiers

RxCUI
1665088 1665093
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 ANDA065441 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (25021-121-20) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

cefepime hydrochloride (1 g/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"}