Orange Book product · Brand (NDA)
DIPROLENE
BETAMETHASONE DIPROPIONATE
At a glance
Aug 01, 1988
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 01, 1988
38 yr 5 mo ago
Today
Pharmaceutical detail
Active ingredient
BETAMETHASONE DIPROPIONATE
Strength
EQ 0.05% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
LOTION, AUGMENTED
Route
TOPICAL
TE code
Not listed
Application
NDA 019716
Product number
001
Marketing status
DISCN
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.
- 1987DIPROLENE AFBrand (NDA)
NDA 019555 · ORGANON
- 1986DIPROLENEBrand (NDA)
NDA 019408 · SCHERING
- 1984ALPHATREXBrand (NDA)
NDA 019143 · SAVAGE LABS
- 1984BETAMETHASONE DIPROPIONATEBrand (NDA)
NDA 019141 · FOUGERA PHARMS INC
- 1984ALPHATREXBrand (NDA)
NDA 019138 · SAVAGE LABS
- 1984BETAMETHASONE DIPROPIONATEBrand (NDA)
NDA 019137 · FOUGERA PHARMS
- 1984BETAMETHASONE DIPROPIONATEBrand (NDA)
NDA 019136 · PHARMADERM
- 1983DIPROLENEBrand (NDA)
NDA 018741 · ORGANON
- —DIPROSONEBrand (NDA)
NDA 017536 · SCHERING
- —DIPROSONEBrand (NDA)
NDA 017829 · SCHERING
- —DIPROSONEBrand (NDA)
NDA 017781 · SCHERING
- 2026BETAMETHASONE DIPROPIONATEGeneric (ANDA)
ANDA 219348 · AUROBINDO PHARMA LTD
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.
