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Last Updated: March 28, 2024

Details for New Drug Application (NDA): 018922


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NDA 018922 describes LODINE, which is a drug marketed by Wyeth Pharms Inc and is included in two NDAs. Additional details are available on the LODINE profile page.

The generic ingredient in LODINE is etodolac. There are twenty-three drug master file entries for this compound. Thirty-one suppliers are listed for this compound. Additional details are available on the etodolac profile page.
Summary for 018922
Tradename:LODINE
Applicant:Wyeth Pharms Inc
Ingredient:etodolac
Patents:0
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 018922

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date:Jan 31, 1991TE:RLD:Yes

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrength300MG
Approval Date:Jan 31, 1991TE:RLD:Yes

Profile for product number 004

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date:Jul 29, 1993TE:RLD:Yes

Expired US Patents for NDA 018922

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Wyeth Pharms Inc LODINE etodolac CAPSULE;ORAL 018922-002 Jan 31, 1991 ⤷  Try a Trial ⤷  Try a Trial
Wyeth Pharms Inc LODINE etodolac CAPSULE;ORAL 018922-002 Jan 31, 1991 ⤷  Try a Trial ⤷  Try a Trial
Wyeth Pharms Inc LODINE etodolac TABLET;ORAL 018922-004 Jul 29, 1993 ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

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