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01 11Indoco Remedies Limited

02 5MSN Laboratories

03 1SHANDONG LUNING PHARMACEUTICAL CO., LTD

04 39Takeda Pharmaceutical

05 6Takeda Pharmaceuticals Australia Pty. Ltd.

06 5Torrent Pharmaceuticals Limited

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PharmaCompass

01

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE

Brand Name : ALOGLIPTIN

Dosage Form : TABLET;ORAL

Dosage Strength : 6.25MG

Packaging :

Approval Date :

Application Number : 210002

Regulatory Info :

Registration Country : USA

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02

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN AND METFORMIN HYDROCHLORIDE

Brand Name : ALOGLIPTIN AND METFORMIN HYDROCHLORIDE

Dosage Form : TABLET; ORAL

Dosage Strength : 12.5MG/500MG

Packaging :

Approval Date :

Application Number : 210212

Regulatory Info :

Registration Country : USA

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03

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN AND METFORMIN HYDROCHLORIDE

Brand Name : ALOGLIPTIN AND METFORMIN HYDROCHLORIDE

Dosage Form : TABLET; ORAL

Dosage Strength : 12.5MG/1000MG

Packaging :

Approval Date :

Application Number : 210212

Regulatory Info :

Registration Country : USA

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04

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE

Brand Name : ALOGLIPTIN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 6.25MG BASE

Packaging :

Approval Date :

Application Number : 210213

Regulatory Info :

Registration Country : USA

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05

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE

Brand Name : ALOGLIPTIN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 12.5MG BASE

Packaging :

Approval Date :

Application Number : 210213

Regulatory Info :

Registration Country : USA

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06

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE

Brand Name : ALOGLIPTIN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date :

Application Number : 210213

Regulatory Info :

Registration Country : USA

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07

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE

Brand Name : NESINA

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 6.25MG BASE

Packaging :

Approval Date : 2013-01-25

Application Number : 22271

Regulatory Info : RX

Registration Country : USA

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08

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE

Brand Name : NESINA

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 12.5MG BASE

Packaging :

Approval Date : 2013-01-25

Application Number : 22271

Regulatory Info : RX

Registration Country : USA

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09

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE

Brand Name : NESINA

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 2013-01-25

Application Number : 22271

Regulatory Info : RX

Registration Country : USA

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10

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE

Brand Name : OSENI

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE;EQ 15MG BASE

Packaging :

Approval Date : 2013-01-25

Application Number : 22426

Regulatory Info : RX

Registration Country : USA

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11

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE

Brand Name : OSENI

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE;EQ 30MG BASE

Packaging :

Approval Date : 2013-01-25

Application Number : 22426

Regulatory Info : RX

Registration Country : USA

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12

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE

Brand Name : OSENI

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE;EQ 45MG BASE

Packaging :

Approval Date : 2013-01-25

Application Number : 22426

Regulatory Info : RX

Registration Country : USA

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13

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE

Brand Name : OSENI

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 12.5MG BASE;EQ 15MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2013-01-25

Application Number : 22426

Regulatory Info : DISCN

Registration Country : USA

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14

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE

Brand Name : OSENI

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 12.5MG BASE;EQ 30MG BASE

Packaging :

Approval Date : 2013-01-25

Application Number : 22426

Regulatory Info : RX

Registration Country : USA

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15

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE

Brand Name : OSENI

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 12.5MG BASE;EQ 45MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2013-01-25

Application Number : 22426

Regulatory Info : DISCN

Registration Country : USA

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16

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE

Brand Name : KAZANO

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 12.5MG BASE;500MG

Packaging :

Approval Date : 2013-01-25

Application Number : 203414

Regulatory Info : RX

Registration Country : USA

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17

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE

Brand Name : KAZANO

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 12.5MG BASE;1GM

Packaging :

Approval Date : 2013-01-25

Application Number : 203414

Regulatory Info : RX

Registration Country : USA

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18

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

alogliptinbensoat

Brand Name : Vipidia

Dosage Form : FILMDRAGERAD TABLETT

Dosage Strength : 6,25 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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19

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN; METFORMIN HYDROCHLORIDE

Brand Name : ALOGLIPTIN; METFORMIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 12.5MG BASE;500MG

Packaging :

Approval Date :

Application Number : 210160

Regulatory Info :

Registration Country : USA

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20

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ALOGLIPTIN; METFORMIN HYDROCHLORIDE

Brand Name : ALOGLIPTIN; METFORMIN HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 12.5MG BASE;1GM

Packaging :

Approval Date :

Application Number : 210160

Regulatory Info :

Registration Country : USA

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