Orange Book product · Generic (ANDA)
MEPROBAMATE
MEPROBAMATE
At a glance
Mar 18, 1982
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Mar 18, 1982
44 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
MEPROBAMATE
Strength
200MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 087825
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of MEPROBAMATE
- —MEPROSPANBrand (NDA)
NDA 011284 · MEDPOINTE PHARM HLC
- —EQUANILBrand (NDA)
NDA 012455 · WYETH AYERST
- —EQUANILBrand (NDA)
NDA 010028 · WYETH AYERST
- —MEPRIAMBrand (NDA)
NDA 016069 · TEVA
- —MEPROBAMATEBrand (NDA)
NDA 014882 · CHARTWELL MOLECULAR
- —MEPROBAMATEBrand (NDA)
NDA 015426 · ELKINS SINN
- —MEPROBAMATEBrand (NDA)
NDA 016928 · HEATHER
- —MEPROBAMATEBrand (NDA)
NDA 014322 · IMPAX LABS
- —MEPROBAMATEBrand (NDA)
NDA 015438 · IVAX SUB TEVA PHARMS
- —MEPROBAMATEBrand (NDA)
NDA 015072 · MALLARD
- —MEPROBAMATEBrand (NDA)
NDA 014368 · MK LABS
- —MEPROBAMATEBrand (NDA)
NDA 014601 · PVT FORM
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.
