Orange Book product · Generic (ANDA)
MECLOFENAMATE SODIUM
MECLOFENAMATE SODIUM
At a glance
Mar 10, 1988
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Mar 10, 1988
38 yr 10 mo ago
Today
Pharmaceutical detail
Active ingredient
MECLOFENAMATE SODIUM
Strength
EQ 100MG BASE
Dosage form
CAPSULE
Route
ORAL
TE code
Not listed
Application
ANDA 072078
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of MECLOFENAMATE SODIUM
- —MECLOMENBrand (NDA)
NDA 018006 · PARKE DAVIS
- 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
- 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.

