Orange Book product · Generic (ANDA)
SULFACETAMIDE SODIUM
SULFACETAMIDE SODIUM
At a glance
Mar 23, 2009
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Mar 23, 2009
17 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
SULFACETAMIDE SODIUM
Strength
10%
Dosage form
LOTION
Route
TOPICAL
TE code
AB
Application
ANDA 078649
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of SULFACETAMIDE SODIUM
- 1996KLARONBrand (NDA)
NDA 019931 · BAUSCH
- —SODIUM SULAMYDBrand (NDA)
NDA 005963 · SCHERING
- 2009SULFACETAMIDE SODIUMGeneric (ANDA)
ANDA 078668 · SUN PHARMA CANADA
- 2006SULFACETAMIDE SODIUMGeneric (ANDA)
ANDA 077015 · FOUGERA PHARMS
- 1999SULFACETAMIDE SODIUMGeneric (ANDA)
ANDA 040216 · EPIC PHARMA LLC
- 1999SULFACETAMIDE SODIUMGeneric (ANDA)
ANDA 040215 · PHARMOBEDIENT
- 1995SULF-15Generic (ANDA)
ANDA 089047 · NOVARTIS
- 1994SULFACETAMIDE SODIUMGeneric (ANDA)
ANDA 040066 · BAUSCH AND LOMB
- 1988SULFACETAMIDE SODIUMGeneric (ANDA)
ANDA 089560 · CHARTWELL RX
- 1987SULFACETAMIDE SODIUMGeneric (ANDA)
ANDA 089068 · ALCON PHARMS LTD
- 1985SULFACETAMIDE SODIUMGeneric (ANDA)
ANDA 088947 · PHARMAFAIR
- 1983SULFAIR FORTEGeneric (ANDA)
ANDA 088385 · PHARMAFAIR
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.
