01 1ACTAVIS ELIZABETH
02 2ADAPTIS
03 2AMNEAL PHARMS CO
04 1ANDA REPOSITORY
05 11ANI PHARMS
06 4APOTEX
07 2BIOPHARM
08 3CHARTWELL MOLECULES
09 4IPCA LABS LTD
10 2IVAX SUB TEVA PHARMS
11 4MYLAN
12 4NATCO PHARMA
13 2OXFORD PHARMS
14 2PANGEA
15 2RANBAXY LABS LTD
16 2SANDOZ
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 : 1997-07-11
Application Number : 74839
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ETODOLAC
Dosage Form : TABLET;ORAL
Dosage Strength : 400MG
Approval Date : 1997-02-28
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 : 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Dosage Strength : 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
