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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

BePharma
Not Confirmed
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BePharma
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

BePharma
Not Confirmed
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BePharma
Not Confirmed

ILOPERIDONE

Brand Name : ILOPERIDONE

Dosage Form : TABLET;ORAL

Dosage Strength : 4MG

Packaging :

Approval Date :

Application Number : 207409

Regulatory Info :

Registration Country : USA

blank

03

BePharma
Not Confirmed
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BePharma
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

BePharma
Not Confirmed
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BePharma
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

blank

05

BePharma
Not Confirmed
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arrow
BePharma
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

blank

06

BePharma
Not Confirmed
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BePharma
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

blank

07

BePharma
Not Confirmed
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BePharma
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

blank

08

BePharma
Not Confirmed
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BePharma
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

BePharma
Not Confirmed
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arrow
BePharma
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

blank

10

BePharma
Not Confirmed
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arrow
BePharma
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

blank

11

BePharma
Not Confirmed
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arrow
BePharma
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

blank

12

BePharma
Not Confirmed
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BePharma
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

blank

13

BePharma
Not Confirmed
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BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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

BePharma
Not Confirmed
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BePharma
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

blank

18

BePharma
Not Confirmed
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BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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

BePharma
Not Confirmed
arrow
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BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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

BePharma
Not Confirmed
arrow
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BePharma
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

BePharma
Not Confirmed
arrow
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BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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

BePharma
Not Confirmed
arrow
arrow
BePharma
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