Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
01 7Taro Pharmaceutical Industries
02 1Octavius Pharma Pvt. Ltd
03 11ANI Pharmaceuticals Inc
04 1Abdi Ibrahim
05 1Acme Lifetech
06 6Actavis Inc
07 5Alfasigma
08 2Amneal Pharmaceuticals
09 4Apotex Inc
10 3Ascent Innovative Medicines
11 2Aspire Lifesciences Pvt Ltd
12 5Bayshore Pharmaceuticals
13 2Biopharm
14 3Chartwell Pharmaceuticals llc
15 2Edenbridge Pharmaceuticals
16 2Humanis
17 2IVAX Pharmaceuticals Inc
18 6Ipca Laboratories
19 3Myungmoon Pharm. Co., LTD.
20 4Natco Pharma
21 5Nobel Ilac Sanayii Ve Ticaret A.S.
22 2Nobel Pharmaceuticals
23 2Oxford Pharm
24 2Pangea Biomed
25 2RANBAXY LABORATORIES LIMITED
26 2SHREE HARI INTL
27 2Sandoz B2B
28 7Teva Pharmaceutical Industries
29 4Viatris
30 7Wyeth Pharmaceuticals Inc
31 2XL Laboratories Private Limited
32 3Zydus Pharmaceuticals
01 2CAPSULE
02 25CAPSULE;ORAL
03 1DC Granules
04 3ER Tablet
05 6Film Coated Tablet
06 1Film-Coated Tablet
07 1Film-Coated Tablets
08 1Filmtable
09 2Granules
10 4Ret Filmtabl
11 1SR Extended Release Tablet
12 5TABLET
13 21TABLET, EXTENDED RELEASE;ORAL
14 37TABLET;ORAL
15 2Tablet
01 49DISCN
02 1DMF Available|FDF Compliance-USP
03 7Generic
04 1Generic B.E study
05 2Generic CTD, ACTD, BE
06 34RX
07 18Blank
01 2CUDIP
02 76ETODOLAC
03 1Etodin
04 2Etodolac
05 2Etodolac NOBEL retard
06 4Etol
07 1Etolax
08 2Etotac SR
09 2Etova
10 4LODINE
11 3LODINE XL
12 3Lodine 300
13 2Lodine Retard
14 8Blank
01 11India
02 3South Korea
03 7Switzerland
04 8Turkey
05 83USA
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info : DMF Available|FDF Compliance-USP
Registration Country : India
Brand Name :
Dosage Form : DC Granules
Dosage Strength : 400MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : DMF Available|FDF Compliance-USP
Registration Country : India
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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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