Application 021341

Type
NDA
Sponsor
GD SEARLE

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
002BEXTRAVALDECOXIBTABLET;ORAL10MGNoNo
003BEXTRAVALDECOXIBTABLET;ORAL20MGNoNo

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

Orange Book products#

Current product rows page 1 of 1 · 2 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N021341-002BEXTRAVALDECOXIB10MGTABLET / ORAL2001-11-16
N021341-003BEXTRAVALDECOXIB20MGTABLET / ORAL2001-11-16

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 3 of 3 · 88 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2022-10-28 04:53 UTC2022-10N021341-002BEXTRA10MGTABLET / ORAL2001-11-16f41ea6bd6efb…
2022-10-28 04:53 UTC2022-10N021341-003BEXTRA20MGTABLET / ORAL2001-11-16f41ea6bd6efb…
2022-09-29 23:25 UTC2022-09N021341-002BEXTRA10MGTABLET / ORAL2001-11-16e64feba35796…
2022-09-29 23:25 UTC2022-09N021341-003BEXTRA20MGTABLET / ORAL2001-11-16e64feba35796…
2022-07-09 03:26 UTC · 3 captures of this ZIP2022-07N021341-002BEXTRA10MGTABLET / ORAL2001-11-16cb3db0bc1861…
2022-07-09 03:26 UTC · 3 captures of this ZIP2022-07N021341-003BEXTRA20MGTABLET / ORAL2001-11-16cb3db0bc1861…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06N021341-002BEXTRA10MGTABLET / ORAL2001-11-16a50c72e98297…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06N021341-003BEXTRA20MGTABLET / ORAL2001-11-16a50c72e98297…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
42110SUPPL2007-01-10
36691SUPPL2004-12-03
27519SUPPL2004-12-02
36690SUPPL2004-05-04
27518SUPPL2004-04-29
23646ORIG2003-12-09
5084SUPPL2002-11-01
42109ORIG2002-05-30
27517ORIG2001-11-16
15219ORIG2001-11-16