Package 25021-122-50

Brand: cefepime

Generic: cefepime hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-122-50
Digits Only 2502112250
Product NDC 25021-122
Description

10 VIAL in 1 CARTON (25021-122-50) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2008-05-01
Brand cefepime
Generic cefepime hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["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 (25021-122-50)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "25021-122-50", "marketing_start_date": "20080501"}], "brand_name": "cefepime", "product_id": "25021-122_a980a9e1-16f8-41c8-a8e4-31101948966c", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "25021-122", "generic_name": "cefepime hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "cefepime", "active_ingredients": [{"name": "CEFEPIME HYDROCHLORIDE", "strength": "2 g/1"}], "application_number": "ANDA065441", "marketing_category": "ANDA", "marketing_start_date": "20080501", "listing_expiration_date": "20261231"}