Orange Book product · Brand (NDA)
ELIMITE
PERMETHRIN
At a glance
Aug 25, 1989
Approved
Brand (NDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 25, 1989
37 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
PERMETHRIN
Strength
5%
Dosage form
CREAM
Route
TOPICAL
TE code
AB
Application
NDA 019855
Product number
001
Marketing status
RX
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
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.
- 1990NIXBrand (NDA)
NDA 019918 · MEDTECH PRODUCTS
- 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.
