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NDC 60505-3518-06 Levetiracetam 1000 mg/1 Details

Levetiracetam 1000 mg/1

Levetiracetam is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Apotex Corp.. The primary component is LEVETIRACETAM.

MedlinePlus Drug Summary

Levetiracetam is used alone and along with other medications to control partial-onset seizures (seizures that involve only one part of the brain) in adults, children, and infants 1 month of age or older. Levetiracetam is also used in combination with other medications to treat seizure in adults and children 12 years of age or older with juvenile myoclonic epilepsy. Levetiracetam is also used in combination with other medications to treat primary generalized tonic-clonic seizures (formerly known as a grand mal seizure; seizure that involves the entire body) in adults and children 6 years of age or older with epilepsy. Levetiracetam is in a class of medications called anticonvulsants. It works by decreasing abnormal excitement in the brain.

Related Packages: 60505-3518-06
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Levetiracetam

Product Information

NDC	60505-3518
Product ID	60505-3518_ce4aeb08-98cd-b031-9262-1bccd2f16f95
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Levetiracetam
Proprietary Name Suffix	n/a
Non-Proprietary Name	Levetiracetam
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	1000
Active Ingredient Units	mg/1
Substance Name	LEVETIRACETAM
Labeler Name	Apotex Corp.
Pharmaceutical Class	Decreased Central Nervous System Disorganized Electrical Activity [PE]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA202958
Listing Certified Through	2024-12-31

Package

NDC 60505-3518-06 (60505351806)

Pricing Information	N/A
NDC Package Code	60505-3518-6
Billing NDC	60505351806
Package	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-3518-6)
Marketing Start Date	2015-02-25
NDC Exclude Flag	N