levetiracetam
Generic: levetiracetam
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
levetiracetam
Generic Name
levetiracetam
Labeler
remedyrepack inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
levetiracetam 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3804
Product ID
70518-3804_3b296ca7-548a-49c3-e063-6394a90a1849
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079063
Listing Expiration
2026-12-31
Marketing Start
2023-07-24
Pharmacologic Class
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183804
Hyphenated Format
70518-3804
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA079063 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 10 CUP, UNIT-DOSE in 1 BOX (70518-3804-0) / 10 mL in 1 CUP, UNIT-DOSE (70518-3804-1)
- 10 CUP, UNIT-DOSE in 1 BOX (70518-3804-2) / 25 mL in 1 CUP, UNIT-DOSE (70518-3804-3)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3b296ca7-548a-49c3-e063-6394a90a1849", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["403884"], "spl_set_id": ["74ccc9f1-b957-4b1b-9464-1b5e3318c916"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 CUP, UNIT-DOSE in 1 BOX (70518-3804-0) / 10 mL in 1 CUP, UNIT-DOSE (70518-3804-1)", "package_ndc": "70518-3804-0", "marketing_start_date": "20230724"}, {"sample": false, "description": "10 CUP, UNIT-DOSE in 1 BOX (70518-3804-2) / 25 mL in 1 CUP, UNIT-DOSE (70518-3804-3)", "package_ndc": "70518-3804-2", "marketing_start_date": "20230724"}], "brand_name": "Levetiracetam", "product_id": "70518-3804_3b296ca7-548a-49c3-e063-6394a90a1849", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-3804", "generic_name": "Levetiracetam", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "100 mg/mL"}], "application_number": "ANDA079063", "marketing_category": "ANDA", "marketing_start_date": "20230724", "listing_expiration_date": "20261231"}