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levetiracetam - 68180-116-01 - (levetiracetam)

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Drug Information of levetiracetam

Product NDC: 68180-116
Proprietary Name: levetiracetam
Non Proprietary Name: levetiracetam
Active Ingredient(s): 100    mg/mL & nbsp;   levetiracetam
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of levetiracetam

Product NDC: 68180-116
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090893
Marketing Category: ANDA
Start Marketing Date: 20130125

Package Information of levetiracetam

Package NDC: 68180-116-01
Package Description: 473 mL in 1 BOTTLE (68180-116-01)

NDC Information of levetiracetam

NDC Code 68180-116-01
Proprietary Name levetiracetam
Package Description 473 mL in 1 BOTTLE (68180-116-01)
Product NDC 68180-116
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levetiracetam
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20130125
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, Inc.
Substance Name LEVETIRACETAM
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of levetiracetam


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