Orange Book product · Generic (ANDA)
OXYMETAZOLINE HYDROCHLORIDE
OXYMETAZOLINE HYDROCHLORIDE
Generic (ANDA)ANDA 213584TE ABRX SUN PHARMA CANADA
At a glance
Oct 04, 2021
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 04, 2021
4 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
OXYMETAZOLINE HYDROCHLORIDE
Strength
1%
Dosage form
CREAM
Route
TOPICAL
TE code
AB
Application
ANDA 213584
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of OXYMETAZOLINE HYDROCHLORIDE
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.
