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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
08 3Cipla Medpro South Africa
09 3Eurolab
10 3F. Hoffmann-La Roche
11 2Fujian South Pharmaceutical
12 5Hetero Drugs
13 3MSN Laboratories
14 3Natco Pharma
15 3Natco Pharma (Canada) Inc
16 2Nishchay Pharmaceuticals Pvt. Ltd.
17 1Pharmascience Inc.
18 3Rising Pharmaceuticals Inc
19 3Sandoz B2B
20 3Shilpa Medicare
21 6Sun Pharmaceutical Industries Limited
22 3Tarbis Farma Sl
23 12Teva Pharmaceutical Industries
24 3Tillomed Laboratories Ltd
25 3Zydus Pharmaceuticals
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01 5FCT
02 21Film Coated Tablet
03 6TAB
04 12TABLET
05 41TABLET;ORAL
06 2Tablet
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01 9Authorized
02 9Cancelled
03 18DISCN
04 10Generic
05 3Originator
06 10Prescription
07 23RX
08 3Suspensed
09 2Blank
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01 3APO-ERLOTINIB
02 1Bilura 100
03 1Bilura 150
04 38ERLOTINIB HYDROCHLORIDE
05 1Elnib 100
06 1Elnib 150
07 1Erlocip 100
08 1Erlocip 150
09 1Erlocip 25
10 3Erlotinib Cipla
11 3Erlotinib Sandoz
12 3Erlotinib Sun
13 3Erlotinib Tarbis
14 3Erlotinib Teva
15 3Erlotinib Teva Group
16 3Erlotinib Tillomed
17 3NAT-ERLOTINIB
18 1PMS-ERLOTINIB
19 3TARCEVA
20 3TEVA-ERLOTINIB
21 3Tarceva®
22 1Tarpib 100 mg
23 1Tarpib 150 mg
24 1Tarpib 25 mg
25 2Blank
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01 10Canada
02 2China
03 2India
04 11South Africa
05 21Spain
06 41USA
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ERLOTINIB HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 100MG BASE
Packaging :
Approval Date : 2019-11-05
Application Number : 208488
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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