APPLICATION
NDA021400
TYPE
NDA
ORIGINAL APPROVAL
2003-08-19
LATEST ACTION
2023-03-15
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued
Products
LEVITRA · ReferenceDiscontinued
VARDENAFIL HYDROCHLORIDE EQ 2.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TABLET · ORAL
LEVITRA · ReferenceDiscontinued
VARDENAFIL HYDROCHLORIDE EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TABLET · ORAL
LEVITRA · ReferenceDiscontinued
VARDENAFIL HYDROCHLORIDE EQ 20MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TABLET · ORAL
LEVITRA · ReferenceDiscontinued
VARDENAFIL HYDROCHLORIDE EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TABLET · ORAL
Approval history
2014-11-03Manufacturing (CMC) · Supplement 18 · standardAP
2003-08-19Type 1 - New Molecular Entity · Original · standard — Other Important Information from FDA ↗AP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
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