01 1ACTAVIS ELIZABETH
02 2ADAPTIS
03 2AMNEAL PHARMS CO
04 11ANI PHARMS
05 4APOTEX
06 2BIOPHARM
07 3CHARTWELL MOLECULES
08 4IPCA LABS LTD
09 2IVAX SUB TEVA PHARMS
10 4MYLAN
11 4NATCO PHARMA
12 2OXFORD PHARMS
13 2PANGEA
14 2RANBAXY LABS LTD
15 2SANDOZ
16 1SENORES PHARMS
17 1SHREE HARI INTL
18 5TARO
19 2TARO PHARM INDS
20 7TEVA
21 5UNICHEM
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 :
Brand Name : ETODOLAC
Dosage Form : TABLET;ORAL
Dosage Strength : 400MG
Approval Date : 1997-02-28
Application Number : 74819
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ETODOLAC
Dosage Form : TABLET;ORAL
Dosage Strength : 500MG
Approval Date : 1998-04-28
Application Number : 74819
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ETODOLAC
Dosage Form : TABLET;ORAL
Dosage Strength : 400MG
Approval Date : 1997-07-11
Application Number : 74839
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
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Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-06-28
Application Number : 18922
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
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Dosage Strength : 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1996-10-25
Application Number : 20584
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
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**
Approval Date : 1996-10-25
Application Number : 20584
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
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**
Approval Date : 1998-01-20
Application Number : 20584
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
