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01 1Alkem Laboratories

02 2Auro Pharma Inc

03 3Aurobindo Pharma Limited

04 1Bionpharma

05 1Chartwell Pharmaceuticals llc

06 3Eisai

07 18Eisai Inc

08 2Glenmark Pharmaceuticals

09 3Hetero Drugs

10 3Hikma Pharmaceuticals

11 4Lupin Ltd

12 1MSN Laboratories

13 2Micro Labs Limited

14 2Norvium

15 1ORIFARM GROUP AS

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PharmaCompass

01

ACS GCI
Not Confirmed
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ACS GCI
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 40MG/ML

Packaging :

Approval Date : 2021-02-23

Application Number : 213410

Regulatory Info : RX

Registration Country : USA

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02

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 40MG/ML

Packaging :

Approval Date : 2019-04-23

Application Number : 211388

Regulatory Info : RX

Registration Country : USA

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03

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 40MG/ML

Packaging :

Approval Date : 2022-11-07

Application Number : 214009

Regulatory Info : RX

Registration Country : USA

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04

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : BANZEL

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2008-11-14

Application Number : 21911

Regulatory Info : DISCN

Registration Country : USA

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05

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : BANZEL

Dosage Form : TABLET;ORAL

Dosage Strength : 200MG

Packaging :

Approval Date : 2008-11-14

Application Number : 21911

Regulatory Info : RX

Registration Country : USA

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06

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : BANZEL

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG

Packaging :

Approval Date : 2008-11-14

Application Number : 21911

Regulatory Info : RX

Registration Country : USA

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07

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : BANZEL

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 40MG/ML

Packaging :

Approval Date : 2011-03-03

Application Number : 201367

Regulatory Info : RX

Registration Country : USA

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08

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 200MG

Packaging :

Approval Date : 2016-05-16

Application Number : 205075

Regulatory Info : RX

Registration Country : USA

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09

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG

Packaging :

Approval Date : 2016-05-16

Application Number : 205075

Regulatory Info : RX

Registration Country : USA

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10

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 200MG

Packaging :

Approval Date : 2021-05-11

Application Number : 204993

Regulatory Info : RX

Registration Country : USA

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11

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG

Packaging :

Approval Date : 2021-05-11

Application Number : 204993

Regulatory Info : RX

Registration Country : USA

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12

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 200MG

Packaging :

Approval Date : 2016-05-16

Application Number : 204988

Regulatory Info : RX

Registration Country : USA

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13

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG

Packaging :

Approval Date : 2016-05-16

Application Number : 204988

Regulatory Info : RX

Registration Country : USA

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14

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 40MG/ML

Packaging :

Approval Date : 2019-04-23

Application Number : 207363

Regulatory Info : RX

Registration Country : USA

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15

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 2022-08-17

Application Number : 204964

Regulatory Info : RX

Registration Country : USA

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16

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 200MG

Packaging :

Approval Date : 2022-08-17

Application Number : 204964

Regulatory Info : RX

Registration Country : USA

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17

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG

Packaging :

Approval Date : 2022-08-17

Application Number : 204964

Regulatory Info : RX

Registration Country : USA

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18

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 40MG/ML

Packaging :

Approval Date : 2020-12-18

Application Number : 213457

Regulatory Info : RX

Registration Country : USA

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19

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 200MG

Packaging :

Approval Date : 2016-05-16

Application Number : 205095

Regulatory Info : RX

Registration Country : USA

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20

Nephrology & Therapeutics
Not Confirmed
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Nephrology & Therapeutics
Not Confirmed

RUFINAMIDE

Brand Name : RUFINAMIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG

Packaging :

Approval Date : 2016-05-16

Application Number : 205095

Regulatory Info : RX

Registration Country : USA

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