Orange Book product · Generic (ANDA)
GLUTETHIMIDE
GLUTETHIMIDE
At a glance
Oct 10, 1986
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 10, 1986
40 yr 3 mo ago
Today
Pharmaceutical detail
Active ingredient
GLUTETHIMIDE
Strength
500MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 089459
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of GLUTETHIMIDE
- —DORIDENBrand (NDA)
NDA 009519 · SANOFI AVENTIS US
- 1986GLUTETHIMIDEGeneric (ANDA)
ANDA 089458 · HALSEY
- —GLUTETHIMIDEGeneric (ANDA)
ANDA 083475 · LANNETT
- —GLUTETHIMIDEGeneric (ANDA)
ANDA 085571 · LANNETT
- —GLUTETHIMIDEGeneric (ANDA)
ANDA 085171 · UCB INC
- —GLUTETHIMIDEGeneric (ANDA)
ANDA 083234 · UPSHER SMITH LABS
- —GLUTETHIMIDEGeneric (ANDA)
ANDA 087297 · VITARINE
- —GLUTETHIMIDEGeneric (ANDA)
ANDA 084362 · WATSON LABS
- —GLUTETHIMIDEGeneric (ANDA)
ANDA 085763 · WATSON LABS
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
