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List of All Manufacturers & Suppliers of Ultradol Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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$ API Ref.Price (USD/KG) : 101Xls
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01 7Taro Pharmaceutical Industries

02 11ANI Pharmaceuticals Inc

03 1Abdi Ibrahim

04 1Acme Lifetech

05 6Actavis Inc

06 5Alfasigma

07 2Amneal Pharmaceuticals

08 4Apotex Inc

09 3Ascent Innovative Medicines

10 2Aspire Lifesciences Pvt Ltd

11 5Bayshore Pharmaceuticals

12 2Biopharm

13 3Chartwell Pharmaceuticals llc

14 2Edenbridge Pharmaceuticals

15 2Humanis

16 2IVAX Pharmaceuticals Inc

17 6Ipca Laboratories

18 3Myungmoon Pharm. Co., LTD.

19 4Natco Pharma

20 5Nobel Ilac Sanayii Ve Ticaret A.S.

21 2Nobel Pharmaceuticals

22 2Oxford Pharm

23 2Pangea Biomed

24 2RANBAXY LABORATORIES LIMITED

25 2SHREE HARI INTL

26 2Sandoz B2B

27 7Teva Pharmaceutical Industries

28 4Viatris

29 7Wyeth Pharmaceuticals Inc

30 2XL Laboratories Private Limited

31 3Zydus Pharmaceuticals

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PharmaCompass

01

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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG

Packaging :

Approval Date : 1998-03-11

Application Number : 75074

Regulatory Info : RX

Registration Country : USA

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02

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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG

Packaging :

Approval Date : 2000-04-25

Application Number : 75074

Regulatory Info : RX

Registration Country : USA

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03

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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : CAPSULE;ORAL

Dosage Strength : 200MG

Packaging :

Approval Date : 1998-04-30

Application Number : 75078

Regulatory Info : RX

Registration Country : USA

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04

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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : CAPSULE;ORAL

Dosage Strength : 300MG

Packaging :

Approval Date : 1998-04-30

Application Number : 75078

Regulatory Info : RX

Registration Country : USA

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05

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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 400MG

Packaging :

Approval Date : 2003-03-13

Application Number : 76174

Regulatory Info : RX

Registration Country : USA

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06

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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 500MG

Packaging :

Approval Date : 2003-03-13

Application Number : 76174

Regulatory Info : RX

Registration Country : USA

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07

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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 600MG

Packaging :

Approval Date : 2003-03-13

Application Number : 76174

Regulatory Info : RX

Registration Country : USA

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08

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : CAPSULE;ORAL

Dosage Strength : 200MG

Packaging :

Approval Date : 1997-08-29

Application Number : 74840

Regulatory Info : DISCN

Registration Country : USA

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09

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : CAPSULE;ORAL

Dosage Strength : 300MG

Packaging :

Approval Date : 1997-08-29

Application Number : 74840

Regulatory Info : DISCN

Registration Country : USA

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10

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG

Packaging :

Approval Date : 1997-06-27

Application Number : 74841

Regulatory Info : DISCN

Registration Country : USA

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11

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG

Packaging :

Approval Date : 1997-02-28

Application Number : 74819

Regulatory Info : DISCN

Registration Country : USA

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12

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG

Packaging :

Approval Date : 1998-04-28

Application Number : 74819

Regulatory Info : DISCN

Registration Country : USA

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13

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : LODINE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1991-01-31

Application Number : 18922

Regulatory Info : DISCN

Registration Country : USA

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14

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : LODINE

Dosage Form : CAPSULE;ORAL

Dosage Strength : 300MG

Packaging :

Approval Date : 1991-01-31

Application Number : 18922

Regulatory Info : DISCN

Registration Country : USA

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15

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : LODINE

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1993-07-29

Application Number : 18922

Regulatory Info : DISCN

Registration Country : USA

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16

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : LODINE

Dosage Form : TABLET;ORAL

Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1996-06-28

Application Number : 18922

Regulatory Info : DISCN

Registration Country : USA

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17

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : LODINE XL

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1996-10-25

Application Number : 20584

Regulatory Info : DISCN

Registration Country : USA

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18

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : LODINE XL

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1996-10-25

Application Number : 20584

Regulatory Info : DISCN

Registration Country : USA

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19

AAPS 2024
Not Confirmed
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : LODINE XL

Dosage Form : TABLET, EXTENDED RELEASE;ORAL

Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1998-01-20

Application Number : 20584

Regulatory Info : DISCN

Registration Country : USA

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20

SHREE HARI INTL

Country
AAPS 2024
Not Confirmed
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SHREE HARI INTL

Country
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AAPS 2024
Not Confirmed

ETODOLAC

Brand Name : ETODOLAC

Dosage Form : TABLET;ORAL

Dosage Strength : 400MG

Packaging :

Approval Date : 1997-07-11

Application Number : 74839

Regulatory Info : DISCN

Registration Country : USA

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