DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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01 1Dr. Reddy's Laboratories
02 1Breckenridge Pharmaceutical
03 2NanoAlvand
04 2Ajanta Pharma Limited
05 2Annora Pharma
06 2Auro Pharma Inc
07 2Aurobindo Pharma Limited
08 2Biocon
09 2Bluepharma
10 3DelNova Healthcare
11 2Devatis AG
12 2Dexcel Pharma
13 2Grindeks AS
14 1Hikma Pharmaceuticals
15 2Intas Pharmaceuticals
16 1JAMP PHARMA
17 2Laboratorio Eczane Pharma
18 2MSN Laboratories
19 1Micro Labs Limited
20 15Pfizer Consumer Healthcare
21 15Pfizer Inc
22 1Pharmascience Inc.
23 3Pluviaendo
24 1Prinston
25 2Pulse Pharmaceuticals
26 4Sandoz B2B
27 1Sinotherapeutics
28 3Taro Pharmaceutical Industries
29 1Unichem Laboratories Limited
30 2Yaopharma
31 3Zydus Pharmaceuticals
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01 3Extended Release Tablet
02 1Extended-Release Tablet
03 1FCT
04 11Film Coated Tablet
05 1Film Coated XR Tablet
06 1Oral Solid Dosage Form
07 2Oral Solution
08 2SOLUTION;ORAL
09 2SR Tablet
10 13TABLET
11 2TABLET (EXTENDED-RELEASE)
12 11TABLET, EXTENDED RELEASE;ORAL
13 11TABLET;ORAL
14 7Tablet
15 11tablet
16 6Blank
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01 6Allowed
02 4Authorized
03 8DISCN
04 1Generic
05 1Lead Market Dossiers- Under Development
06 1Originator
07 12Prescription
08 8RX
09 44Blank
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01 2AURO-TOFACITINIB
02 1JAMP TOFACITINIB
03 1PMS-TOFACITINIB
04 2Rhofanib
05 2SANDOZ TOFACITINIB
06 2TARO-TOFACITINIB
07 1TARO-TOFACITINIB XR
08 7TOFACITINIB
09 13TOFACITINIB CITRATE
10 2Tofacitinib
11 2Tofacitinib Devatis
12 2Tofacitinib Sandoz
13 2Tofax
14 1Tofaxen 11 XR
15 1Tofaxen 5
16 5XELJANZ
17 5XELJANZ XR
18 22Xeljanz
19 1Xeljanz 5 mg
20 11Blank
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01 2Argentina
02 15Australia
03 12Canada
04 9India
05 2Iran
06 2Latvia
07 2Portugal
08 1South Africa
09 4Spain
10 6Switzerland
11 3Turkey
12 27USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Lead Market Dossiers- Under Development
Registration Country : India
Brand Name :
Dosage Form : Oral Solid Dosage Form
Dosage Strength : 22MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Lead Market Dossiers- Under Development
Registration Country : India
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Regulatory Info :
Registration Country : USA
Brand Name : TOFACITINIB
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 209633
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : Iran
Brand Name : Rhofanib
Dosage Form : Film Coated Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
Regulatory Info :
Registration Country : Iran
Brand Name : Rhofanib
Dosage Form : Film Coated Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
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Regulatory Info : DISCN
Registration Country : USA
Brand Name : TOFACITINIB CITRATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2021-06-01
Application Number : 212943
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : TOFACITINIB
Dosage Form : TABLET
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 215356
Regulatory Info :
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : TOFACITINIB CITRATE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 1MG BASE/ML
Packaging :
Approval Date : 2023-09-25
Application Number : 216878
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : TOFACITINIB CITRATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2023-03-13
Application Number : 209738
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : XELJANZ
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2012-11-06
Application Number : 203214
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : XELJANZ
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 10MG BASE
Packaging :
Approval Date : 2018-05-30
Application Number : 203214
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : XELJANZ XR
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 11MG BASE
Packaging :
Approval Date : 2016-02-23
Application Number : 208246
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : XELJANZ XR
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 22MG BASE
Packaging :
Approval Date : 2019-12-12
Application Number : 208246
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : XELJANZ
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 1MG BASE/ML
Packaging :
Approval Date : 2020-09-25
Application Number : 213082
Regulatory Info : RX
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : TOFACITINIB
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 209923
Regulatory Info :
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Brand Name : TOFACITINIB CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 11MG BASE
Packaging :
Approval Date : 2025-09-30
Application Number : 216001
Regulatory Info : RX
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : Tofacitinib
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 215552
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : Tofacitinib
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number : 215552
Regulatory Info :
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : TOFACITINIB CITRATE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2023-03-13
Application Number : 209829
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : TOFACITINIB CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 11MG BASE
Packaging :
Approval Date : 2021-08-19
Application Number : 214264
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
Brand Name : TOFACITINIB CITRATE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 22MG BASE
Packaging :
Approval Date : 2021-08-19
Application Number : 214264
Regulatory Info : DISCN
Registration Country : USA
