Orange Book product · Generic (ANDA)
DEXAMETHASONE
DEXAMETHASONE
At a glance
Apr 28, 1983
Approved
Generic (ANDA)
Application
BP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 28, 1983
43 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
DEXAMETHASONE
Strength
0.5MG
Dosage form
TABLET
Route
ORAL
TE code
BP
Application
ANDA 088481
Product number
002
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of DEXAMETHASONE
- 2018DEXTENZABrand (NDA)
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- 2009OZURDEXBrand (NDA)
NDA 022315 · ABBVIE
- —DECASPRAYBrand (NDA)
NDA 012731 · MERCK
- —DECADRONBrand (NDA)
NDA 012376 · MERCK
- —HEXADROLBrand (NDA)
NDA 012674 · ASPEN GLOBAL INC
- —DECADERMBrand (NDA)
NDA 013538 · MERCK
- —MAXIDEXBrand (NDA)
NDA 013422 · HARROW EYE
- —DECADRONBrand (NDA)
NDA 011664 · MERCK
- 2024DEXAMETHASONEGeneric (ANDA)
ANDA 218372 · COREPHARMA
- 2023DEXAMETHASONEGeneric (ANDA)
ANDA 215604 · NOVITIUM PHARMA
- 2023DEXAMETHASONEGeneric (ANDA)
ANDA 217695 · APOTEX
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.
