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NDC 65162-0529-16 Levetiracetam 500 mg/1 Details

Levetiracetam 500 mg/1

Levetiracetam is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. 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: 65162-0529-16
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Levetiracetam

Product Information

NDC	65162-0529
Product ID	65162-529_fa9c045e-8dbd-49d9-a7f4-7c648c3d2de1
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
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	LEVETIRACETAM
Labeler Name	Amneal Pharmaceuticals LLC
Pharmaceutical Class	Decreased Central Nervous System Disorganized Electrical Activity [PE]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA090767
Listing Certified Through	2024-12-31

Package

NDC 65162-0529-16 (65162052916)

Pricing Information	N/A
NDC Package Code	65162-529-16
Billing NDC	65162052916
Package	120 TABLET, FILM COATED in 1 BOTTLE (65162-529-16)
Marketing Start Date	2013-02-28
NDC Exclude Flag	N