Orange Book product · Brand (NDA)
NIX
PERMETHRIN
At a glance
May 02, 1990
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 02, 1990
36 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
PERMETHRIN
Strength
1%
Dosage form
LOTION
Route
TOPICAL
TE code
Not listed
Application
NDA 019918
Product number
001
Marketing status
OTC
Reference listed drug (RLD)
Yes
Reference standard (RS)
Yes
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
- 1989ELIMITEBrand (NDA)
NDA 019855 · AUROBINDO PHARMA USA
- 1986NIXBrand (NDA)
NDA 019435 · GLAXOSMITHKLINE
- 2023PERMETHRINGeneric (ANDA)
ANDA 209732 · DR REDDYS LABS EU
- 2019PERMETHRINGeneric (ANDA)
ANDA 211303 · ENCUBE ETHICALS
- 2003PERMETHRINGeneric (ANDA)
ANDA 076369 · PADAGIS ISRAEL
- 2001PERMETHRINGeneric (ANDA)
ANDA 076090 · PERRIGO NEW YORK
- 2000PERMETHRINGeneric (ANDA)
ANDA 075014 · ACTAVIS MID ATLANTIC
- 1998PERMETHRINGeneric (ANDA)
ANDA 074806 · ACTAVIS 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.
