01 5TARO
02 2TARO PHARM INDS
03 2ABRAXEOLUS
04 1ACTAVIS ELIZABETH
05 2ADAPTIS
06 2AMNEAL PHARMS CO
07 11ANI PHARMS
08 2APOTEX
09 2APOTEX INC
10 5BAYSHORE PHARMS LLC
11 2BIOPHARM
12 3CHARTWELL MOLECULES
13 4IPCA LABS LTD
14 2IVAX SUB TEVA PHARMS
15 4MYLAN
16 4NATCO PHARMA
17 2OXFORD PHARMS
18 2RANBAXY LABS LTD
19 2SANDOZ
20 2SHREE HARI INTL
21 7TEVA
22 3WATSON LABS
23 2WATSON LABS FLORIDA
24 7WYETH PHARMS INC
25 3ZYDUS PHARMS
01 25CAPSULE;ORAL
02 21TABLET, EXTENDED RELEASE;ORAL
03 37TABLET;ORAL
01 49DISCN
02 34RX
01 76ETODOLAC
02 4LODINE
03 3LODINE XL
01 78No
02 5Yes
RLD : No
TE Code : AB
Brand Name : ETODOLAC
Dosage Form : TABLET;ORAL
Dosage Strength : 400MG
Approval Date : 1998-03-11
Application Number : 75074
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ETODOLAC
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 2000-04-25
Application Number : 75074
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ETODOLAC
Dosage Form : CAPSULE;ORAL
Dosage Strength : 200MG
Approval Date : 1998-04-30
Application Number : 75078
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ETODOLAC
Dosage Form : CAPSULE;ORAL
Dosage Strength : 300MG
Approval Date : 1998-04-30
Application Number : 75078
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ETODOLAC
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 400MG
Approval Date : 2003-03-13
Application Number : 76174
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ETODOLAC
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 500MG
Approval Date : 2003-03-13
Application Number : 76174
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ETODOLAC
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 600MG
Approval Date : 2003-03-13
Application Number : 76174
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
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Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1991-01-31
Application Number : 18922
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : LODINE
Dosage Form : CAPSULE;ORAL
Dosage Strength : 300MG
Approval Date : 1991-01-31
Application Number : 18922
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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**
Approval Date : 1993-07-29
Application Number : 18922
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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