Orange Book product · Generic (ANDA)
DORZOLAMIDE HYDROCHLORIDE
DORZOLAMIDE HYDROCHLORIDE
At a glance
Oct 28, 2008
Approved
Generic (ANDA)
Application
AT
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 28, 2008
17 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
DORZOLAMIDE HYDROCHLORIDE
Strength
EQ 2% BASE
Dosage form
SOLUTION/DROPS
Route
OPHTHALMIC
TE code
AT
Application
ANDA 078395
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of DORZOLAMIDE HYDROCHLORIDE
- 1994TRUSOPTBrand (NDA)
NDA 020408 · MSD SUB MERCK
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ANDA 215004 · SOMERSET THERAPS LLC
- 2022DORZOLAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 215660 · GLAND
- 2019DORZOLAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 204778 · MICRO LABS
- 2019DORZOLAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 212639 · ALEMBIC
- 2019DORZOLAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 205294 · FDC LTD
- 2014DORZOLAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 202053 · REGCON HOLDINGS
- 2013DORZOLAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 091034 · ZAMBON SPA
- 2009DORZOLAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 079186 · AM REGENT
- 2009DORZOLAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 090143 · BAUSCH AND LOMB
- 2009DORZOLAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 078981 · SANDOZ
- 2008DORZOLAMIDE HYDROCHLORIDEGeneric (ANDA)
ANDA 078756 · TEVA PHARMS
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.
