ANDA 078918

ZYDUS PHARMS USA INC

FDA Drug Application

Application #078918

Application Sponsors

ANDA 078918

ZYDUS PHARMS USA INC

Marketing Status

• Prescription: 001
• Prescription: 002

Application Products

001	TABLET;ORAL	250MG	0	LEVETIRACETAM	LEVETIRACETAM
002	TABLET;ORAL	1GM	0	LEVETIRACETAM	LEVETIRACETAM

FDA Submissions

	ORIG	1	AP	2009-04-29
LABELING; Labeling	SUPPL	2	AP	2009-09-15
LABELING; Labeling	SUPPL	3	AP	2010-09-21
LABELING; Labeling	SUPPL	4	AP	2010-11-17
REMS; REMS	SUPPL	6	AP	2011-11-29
LABELING; Labeling	SUPPL	7	AP	2016-02-10
LABELING; Labeling	SUPPL	8	AP	2021-01-11	STANDARD
LABELING; Labeling	SUPPL	9	AP	2021-01-11	STANDARD
LABELING; Labeling	SUPPL	10	AP	2021-01-11	STANDARD

Submissions Property Types

SUPPL	1	Null	7
SUPPL	2	Null	7
SUPPL	3	Null	8
SUPPL	4	Null	8
SUPPL	6	Null	15
SUPPL	7	Null	15
SUPPL	8	Null	15
SUPPL	9	Null	15
SUPPL	10	Null	7

TE Codes

001	Prescription	AB
002	Prescription	AB

CDER Filings

ZYDUS PHARMS USA INC

cder:Array
(
    [0] => Array
        (
            [ApplNo] => 78918
            [companyName] => ZYDUS PHARMS USA INC
            [docInserts] => ["",""]
            [products] => [{"drugName":"LEVETIRACETAM","activeIngredients":"LEVETIRACETAM","strength":"250MG","dosageForm":"TABLET;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"},{"drugName":"LEVETIRACETAM","activeIngredients":"LEVETIRACETAM","strength":"1GM","dosageForm":"TABLET;ORAL","marketingStatus":"Prescription","te":"","rld":"No","rs":"No"}]
            [labels] => 
            [originalApprovals] => [{"actionDate":"LEVETIRACETAM","submission":"LEVETIRACETAM","actionType":"250MG","submissionClassification":"TABLET;ORAL","reviewPriority":"Prescription","inserts":"[]","notes":">No"},{"actionDate":"LEVETIRACETAM","submission":"LEVETIRACETAM","actionType":"1GM","submissionClassification":"TABLET;ORAL","reviewPriority":"Prescription","inserts":"[]","notes":">No"}]
            [supplements] => 
            [actionDate] => 1969-12-31
        )

)