Application 021012

Type
NDA
Sponsor
CIS BIO INTL SA

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001NEO TECT KITTECHNETIUM TC-99M DEPREOTIDEINJECTABLE;INJECTIONN/A **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**NoNo

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

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

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N021012-001NEO TECT KITTECHNETIUM TC-99M DEPREOTIDEN/A **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE / INJECTION1999-08-03

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 2 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2022-09-29 23:25 UTC2022-09N021012-001NEO TECT KITN/A **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE / INJECTION1999-08-03e64feba35796…
2022-07-09 03:26 UTC · 3 captures of this ZIP2022-07N021012-001NEO TECT KITN/A **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE / INJECTION1999-08-03cb3db0bc1861…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06N021012-001NEO TECT KITN/A **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**INJECTABLE / INJECTION1999-08-03a50c72e98297…

Reported adverse events (FAERS/openFDA)#

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

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
35880SUPPL2004-10-08
4033SUPPL2004-10-08
41875ORIG1999-08-03
26482ORIG1999-08-03
14160ORIG1999-08-03