Application 062483

Type
ANDA
Sponsor
VALEANT LUXEMBOURG

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001GRIFULVIN VGRISEOFULVIN, MICROSIZESUSPENSION;ORAL125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**NoNo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 44.

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
A062483-001GRIFULVIN VGRISEOFULVIN, MICROSIZE125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**SUSPENSION / ORAL1984-01-26

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 · 44 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2022-10-28 04:53 UTC2022-10A062483-001GRIFULVIN V125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**SUSPENSION / ORAL1984-01-26f41ea6bd6efb…
2022-09-29 23:25 UTC2022-09A062483-001GRIFULVIN V125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**SUSPENSION / ORAL1984-01-26e64feba35796…
2022-07-09 03:26 UTC · 3 captures of this ZIP2022-07A062483-001GRIFULVIN V125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**SUSPENSION / ORAL1984-01-26cb3db0bc1861…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A062483-001GRIFULVIN V125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**SUSPENSION / ORAL1984-01-26a50c72e98297…

Reported adverse events (FAERS/openFDA)#

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

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
42762SUPPL2005-07-22
22264SUPPL2003-08-05
22263SUPPL2003-08-05
22262SUPPL2003-08-05
22261SUPPL2003-08-05
22260SUPPL2003-08-05
22259SUPPL2003-08-05
22258SUPPL2003-08-05
42761SUPPL2003-07-31
42760SUPPL2003-07-31
22269SUPPL2003-07-31
22268SUPPL2003-07-31
22267SUPPL2003-07-31
22266SUPPL2003-07-31
22265SUPPL2003-07-31
22257ORIG2003-07-31