Orange Book product · Generic (ANDA)
MEPROBAMATE
MEPROBAMATE
At a glance
Feb 18, 2009
Approved
Generic (ANDA)
Application
AA
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 18, 2009
17 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
MEPROBAMATE
Strength
200MG
Dosage form
TABLET
Route
ORAL
TE code
AA
Application
ANDA 090122
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
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.
