ceftazidime
Generic: ceftazidime
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
ceftazidime
Generic Name
ceftazidime
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ceftazidime 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
25021-127
Product ID
25021-127_6b34b5ad-001f-4c39-8415-a223eb692b46
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062640
Listing Expiration
2026-12-31
Marketing Start
2008-05-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021127
Hyphenated Format
25021-127
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
ceftazidime (source: ndc)
Generic Name
ceftazidime (source: ndc)
Application Number
ANDA062640 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 25 VIAL in 1 CARTON (25021-127-20) / 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": "6b34b5ad-001f-4c39-8415-a223eb692b46", "openfda": {"unii": ["9M416Z9QNR"], "rxcui": ["1659283", "1659287"], "spl_set_id": ["112c5457-8d71-49f5-b531-9761d7d38c93"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-127-20) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "25021-127-20", "marketing_start_date": "20080515"}], "brand_name": "Ceftazidime", "product_id": "25021-127_6b34b5ad-001f-4c39-8415-a223eb692b46", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "25021-127", "generic_name": "ceftazidime", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftazidime", "active_ingredients": [{"name": "CEFTAZIDIME", "strength": "1 g/1"}], "application_number": "ANDA062640", "marketing_category": "ANDA", "marketing_start_date": "20080515", "listing_expiration_date": "20261231"}