Orange Book product · Brand (NDA)
MECLOMEN
MECLOFENAMATE SODIUM
At a glance
Approved Prior to Jan 1, 1982
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
MECLOFENAMATE SODIUM
Strength
EQ 100MG BASE
Dosage form
CAPSULE
Route
ORAL
TE code
Not listed
Application
NDA 018006
Product number
002
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 1989MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 072848 · BARR
- 1989MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 072809 · BARR
- 1988MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 072262 · CHARTWELL RX
- 1988MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 072263 · CHARTWELL RX
- 1988MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 071710 · VITARINE
- 1988MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 071684 · VITARINE
- 1988MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 071007 · USL PHARMA
- 1988MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 071008 · USL PHARMA
- 1988MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 072077 · PAR PHARM
- 1988MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 072078 · PAR PHARM
- 1987MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 071640 · WATSON LABS
- 1987MECLOFENAMATE SODIUMGeneric (ANDA)
ANDA 071641 · 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.

