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01 5Alembic Pharmaceuticals Limited

02 14Inventia Healthcare Limited

03 7Lupin Ltd

04 7Taro Pharmaceutical Industries

05 7Vanda Pharmaceuticals

06 28Blank

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PharmaCompass

01

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 2MG

Packaging :

Approval Date :

Application Number : 207409

Regulatory Info :

Registration Country : USA

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02

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 4MG

Packaging :

Approval Date :

Application Number : 207409

Regulatory Info :

Registration Country : USA

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03

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG

Packaging :

Approval Date : 2016-11-28

Application Number : 207231

Regulatory Info : DISCN

Registration Country : USA

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04

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 2MG

Packaging :

Approval Date : 2016-11-28

Application Number : 207231

Regulatory Info : DISCN

Registration Country : USA

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05

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 4MG

Packaging :

Approval Date : 2016-11-28

Application Number : 207231

Regulatory Info : DISCN

Registration Country : USA

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06

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 6MG

Packaging :

Approval Date : 2016-11-28

Application Number : 207231

Regulatory Info : DISCN

Registration Country : USA

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07

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 8MG

Packaging :

Approval Date : 2016-11-28

Application Number : 207231

Regulatory Info : DISCN

Registration Country : USA

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08

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2016-11-28

Application Number : 207231

Regulatory Info : DISCN

Registration Country : USA

blank

09

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 12MG

Packaging :

Approval Date : 2016-11-28

Application Number : 207231

Regulatory Info : DISCN

Registration Country : USA

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10

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG

Packaging :

Approval Date : 2022-05-05

Application Number : 206890

Regulatory Info : DISCN

Registration Country : USA

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11

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 2MG

Packaging :

Approval Date : 2022-05-05

Application Number : 206890

Regulatory Info : DISCN

Registration Country : USA

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12

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 4MG

Packaging :

Approval Date : 2022-05-05

Application Number : 206890

Regulatory Info : DISCN

Registration Country : USA

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13

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 6MG

Packaging :

Approval Date : 2022-05-05

Application Number : 206890

Regulatory Info : DISCN

Registration Country : USA

blank

14

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 8MG

Packaging :

Approval Date : 2022-05-05

Application Number : 206890

Regulatory Info : DISCN

Registration Country : USA

blank

15

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2022-05-05

Application Number : 206890

Regulatory Info : DISCN

Registration Country : USA

blank

16

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 12MG

Packaging :

Approval Date : 2022-05-05

Application Number : 206890

Regulatory Info : DISCN

Registration Country : USA

blank

17

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG

Packaging :

Approval Date : 2019-07-22

Application Number : 207098

Regulatory Info : DISCN

Registration Country : USA

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18

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 2MG

Packaging :

Approval Date : 2019-07-22

Application Number : 207098

Regulatory Info : DISCN

Registration Country : USA

blank

19

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 4MG

Packaging :

Approval Date : 2019-07-22

Application Number : 207098

Regulatory Info : DISCN

Registration Country : USA

blank

20

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 6MG

Packaging :

Approval Date : 2019-07-22

Application Number : 207098

Regulatory Info : DISCN

Registration Country : USA

blank

21

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 8MG

Packaging :

Approval Date : 2019-07-22

Application Number : 207098

Regulatory Info : DISCN

Registration Country : USA

blank

22

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2019-07-22

Application Number : 207098

Regulatory Info : DISCN

Registration Country : USA

blank

23

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 12MG

Packaging :

Approval Date : 2019-07-22

Application Number : 207098

Regulatory Info : DISCN

Registration Country : USA

blank

24

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : FANAPT

Dosage Form : TABLET;ORAL

Dosage Strength : 1MG

Packaging :

Approval Date : 2009-05-06

Application Number : 22192

Regulatory Info : RX

Registration Country : USA

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25

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : FANAPT

Dosage Form : TABLET;ORAL

Dosage Strength : 2MG

Packaging :

Approval Date : 2009-05-06

Application Number : 22192

Regulatory Info : RX

Registration Country : USA

blank

26

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : FANAPT

Dosage Form : TABLET;ORAL

Dosage Strength : 4MG

Packaging :

Approval Date : 2009-05-06

Application Number : 22192

Regulatory Info : RX

Registration Country : USA

blank

27

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : FANAPT

Dosage Form : TABLET;ORAL

Dosage Strength : 6MG

Packaging :

Approval Date : 2009-05-06

Application Number : 22192

Regulatory Info : RX

Registration Country : USA

blank

28

PharmaVenue
Not Confirmed
arrow
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : FANAPT

Dosage Form : TABLET;ORAL

Dosage Strength : 8MG

Packaging :

Approval Date : 2009-05-06

Application Number : 22192

Regulatory Info : RX

Registration Country : USA

blank

29

PharmaVenue
Not Confirmed
arrow
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : FANAPT

Dosage Form : TABLET;ORAL

Dosage Strength : 10MG

Packaging :

Approval Date : 2009-05-06

Application Number : 22192

Regulatory Info : RX

Registration Country : USA

blank

30

PharmaVenue
Not Confirmed
arrow
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PharmaVenue
Not Confirmed

ILOPERIDONE

Brand Name : FANAPT

Dosage Form : TABLET;ORAL

Dosage Strength : 12MG

Packaging :

Approval Date : 2009-05-06

Application Number : 22192

Regulatory Info : RX

Registration Country : USA

blank