levetiracetam
Generic: levetiracetam
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
levetiracetam
Generic Name
levetiracetam
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Routes
Active Ingredients
levetiracetam 500 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-780
Product ID
25021-780_71dae9d8-f833-46d3-9b2a-c7760742f412
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091627
Listing Expiration
2026-12-31
Marketing Start
2013-11-01
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021780
Hyphenated Format
25021-780
Supplemental Identifiers
RxCUI
UNII
NUI
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
levetiracetam (source: ndc)
Generic Name
levetiracetam (source: ndc)
Application Number
ANDA091627 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/5mL
Packaging
- 10 VIAL in 1 CARTON (25021-780-05) / 5 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "71dae9d8-f833-46d3-9b2a-c7760742f412", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["647121"], "spl_set_id": ["f00d8f59-c333-48ad-aca3-98a49bcd228e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-780-05) / 5 mL in 1 VIAL", "package_ndc": "25021-780-05", "marketing_start_date": "20131101"}], "brand_name": "Levetiracetam", "product_id": "25021-780_71dae9d8-f833-46d3-9b2a-c7760742f412", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "25021-780", "generic_name": "Levetiracetam", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/5mL"}], "application_number": "ANDA091627", "marketing_category": "ANDA", "marketing_start_date": "20131101", "listing_expiration_date": "20261231"}