Orange Book product · Generic (ANDA)
TOLMETIN SODIUM
TOLMETIN SODIUM
At a glance
May 27, 1993
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 27, 1993
33 yr 7 mo ago
Today
Pharmaceutical detail
Active ingredient
TOLMETIN SODIUM
Strength
EQ 400MG BASE
Dosage form
CAPSULE
Route
ORAL
TE code
Not listed
Application
ANDA 073393
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of TOLMETIN SODIUM
- —TOLECTIN DSBrand (NDA)
NDA 018084 · ORTHO MCNEIL JANSSEN
- —TOLECTINBrand (NDA)
NDA 017628 · ORTHO MCNEIL JANSSEN
- 1997TOLMETIN SODIUMGeneric (ANDA)
ANDA 074729 · COSETTE
- 1996TOLMETIN SODIUMGeneric (ANDA)
ANDA 074399 · COSETTE
- 1994TOLMETIN SODIUMGeneric (ANDA)
ANDA 074473 · RISING
- 1993TOLMETIN SODIUMGeneric (ANDA)
ANDA 074002 · CHARTWELL RX
- 1992TOLMETIN SODIUMGeneric (ANDA)
ANDA 073588 · CHARTWELL RX
- 1992TOLMETIN SODIUMGeneric (ANDA)
ANDA 073527 · ANI PHARMS
- 1992TOLMETIN SODIUMGeneric (ANDA)
ANDA 073519 · ANI PHARMS
- 1992TOLMETIN SODIUMGeneric (ANDA)
ANDA 073462 · CHARTWELL RX
- 1992TOLMETIN SODIUMGeneric (ANDA)
ANDA 073308 · ANI PHARMS
- 1992TOLMETIN SODIUMGeneric (ANDA)
ANDA 073392 · ANI PHARMS
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.
