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Levetiracetam - 68094-816-62 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 68094-816
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 500    mg/5mL & nbsp;   Levetiracetam
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 68094-816
Labeler Name: Precision Dose Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090992
Marketing Category: ANDA
Start Marketing Date: 20111208

Package Information of Levetiracetam

Package NDC: 68094-816-62
Package Description: 3 TRAY in 1 CASE (68094-816-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-816-59)

NDC Information of Levetiracetam

NDC Code 68094-816-62
Proprietary Name Levetiracetam
Package Description 3 TRAY in 1 CASE (68094-816-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-816-59)
Product NDC 68094-816
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20111208
Marketing Category Name ANDA
Labeler Name Precision Dose Inc.
Substance Name LEVETIRACETAM
Strength Number 500
Strength Unit mg/5mL
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Levetiracetam


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