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NDC 68788-7430-01 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 Preferred Pharmaceuticals, Inc.. 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: 68788-7430-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Levetiracetam

Product Information

NDC	68788-7430
Product ID	68788-7430_33fb6506-f36e-41f3-8085-36c833b150e1
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	Preferred Pharmaceuticals, Inc.
Pharmaceutical Class	Decreased Central Nervous System Disorganized Electrical Activity [PE]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA090515
Listing Certified Through	2024-12-31

Package

NDC 68788-7430-01 (68788743001)

Pricing Information	N/A
NDC Package Code	68788-7430-1
Billing NDC	68788743001
Package	100 TABLET, FILM COATED in 1 BOTTLE (68788-7430-1)
Marketing Start Date	2019-10-02
NDC Exclude Flag	N