levetiracetam

Generic: levetiracetam

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levetiracetam
Generic Name levetiracetam
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levetiracetam 750 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4013
Product ID 70518-4013_42b409f9-1b55-2e47-e063-6394a90a2700
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091491
Listing Expiration 2026-12-31
Marketing Start 2024-02-07

Pharmacologic Class

Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184013
Hyphenated Format 70518-4013

Supplemental Identifiers

RxCUI
311290
UNII
44YRR34555
NUI
N0000008486

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 ANDA091491 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-4013-0)
source: ndc

Packages (1)

70518-4013-0 30 TABLET in 1 BLISTER PACK (70518-4013-0)

Ingredients (1)

levetiracetam (750 mg/1)

Linked Drug Pages (1)

Levetiracetam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42b409f9-1b55-2e47-e063-6394a90a2700", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311290"], "spl_set_id": ["a05bbfa4-c34f-4134-8207-db79e4c70445"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4013-0)", "package_ndc": "70518-4013-0", "marketing_start_date": "20250207"}], "brand_name": "Levetiracetam", "product_id": "70518-4013_42b409f9-1b55-2e47-e063-6394a90a2700", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4013", "generic_name": "Levetiracetam", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "750 mg/1"}], "application_number": "ANDA091491", "marketing_category": "ANDA", "marketing_start_date": "20240207", "listing_expiration_date": "20261231"}