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01 3Accord healthcare

02 3Alembic Pharmaceuticals Limited

03 6Apotex Inc

04 3Astellas Pharma

05 3Aurobindo Pharma Limited

06 2Chartwell Pharmaceuticals llc

07 3Cipla Medpro South Africa

08 3Eurolab

09 6F. Hoffmann-La Roche

10 2Fujian South Pharmaceutical

11 5Hetero Drugs

12 3MSN Laboratories

13 3Natco Pharma

14 3Natco Pharma (Canada) Inc

15 2Nishchay Pharmaceuticals Pvt. Ltd.

16 2Pharmascience Inc.

17 3Rising Pharmaceuticals Inc

18 3Shilpa Medicare

19 3Sun Pharmaceutical Industries Limited

20 6Teva Pharmaceutical Industries

21 3Zydus Pharmaceuticals

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PharmaCompass

01

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 2019-11-05

Application Number : 208396

Regulatory Info : DISCN

Registration Country : USA

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02

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2019-11-05

Application Number : 208396

Regulatory Info : DISCN

Registration Country : USA

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03

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2019-11-05

Application Number : 208396

Regulatory Info : DISCN

Registration Country : USA

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04

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : TARCEVA

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2004-11-18

Application Number : 21743

Regulatory Info : DISCN

Registration Country : USA

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05

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : TARCEVA

Dosage Form : TABLET;ORAL

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

Packaging :

Approval Date : 2004-11-18

Application Number : 21743

Regulatory Info : DISCN

Registration Country : USA

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06

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : TARCEVA

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2004-11-18

Application Number : 21743

Regulatory Info : DISCN

Registration Country : USA

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07

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 2024-09-13

Application Number : 203843

Regulatory Info : RX

Registration Country : USA

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08

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2024-09-13

Application Number : 203843

Regulatory Info : RX

Registration Country : USA

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09

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 2024-05-24

Application Number : 209267

Regulatory Info : RX

Registration Country : USA

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10

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2024-05-24

Application Number : 209267

Regulatory Info : RX

Registration Country : USA

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11

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2024-05-24

Application Number : 209267

Regulatory Info : RX

Registration Country : USA

blank

12

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 2019-11-05

Application Number : 208488

Regulatory Info : DISCN

Registration Country : USA

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13

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2019-11-05

Application Number : 208488

Regulatory Info : RX

Registration Country : USA

blank

14

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2019-11-05

Application Number : 208488

Regulatory Info : DISCN

Registration Country : USA

blank

15

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 2014-06-11

Application Number : 91002

Regulatory Info : RX

Registration Country : USA

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16

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2014-06-11

Application Number : 91002

Regulatory Info : RX

Registration Country : USA

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17

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2014-06-11

Application Number : 91002

Regulatory Info : RX

Registration Country : USA

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18

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 25MG BASE

Packaging :

Approval Date : 2020-11-09

Application Number : 91059

Regulatory Info : RX

Registration Country : USA

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19

AACR Annual meeting
Not Confirmed
arrow
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AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 100MG BASE

Packaging :

Approval Date : 2015-08-28

Application Number : 91059

Regulatory Info : RX

Registration Country : USA

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20

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

ERLOTINIB HYDROCHLORIDE

Brand Name : ERLOTINIB HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 150MG BASE

Packaging :

Approval Date : 2015-08-28

Application Number : 91059

Regulatory Info : RX

Registration Country : USA

blank