Orange Book product · Brand (NDA)
MINIPRESS XL
PRAZOSIN HYDROCHLORIDE
At a glance
Jan 29, 1992
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 29, 1992
34 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
PRAZOSIN HYDROCHLORIDE
Strength
2.5MG
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
TE code
Not listed
Application
NDA 019775
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- —MINIPRESSBrand (NDA)
NDA 017442 · PFIZER
- 2024PRAZOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 216727 · MSN
- 2024PRAZOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 214083 · LANNETT CO INC
- 2023PRAZOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 213052 · AUROBINDO PHARMA LTD
- 2023PRAZOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 217268 · ALEMBIC
- 2022PRAZOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 215697 · MANKIND PHARMA
- 2022PRAZOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 213406 · APPCO
- 2021PRAZOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 214608 · GRANULES
- 2018PRAZOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 210971 · NOVITIUM PHARMA
- 1989PRAZOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 072782 · AM THERAP
- 1989PRAZOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 072783 · AM THERAP
- 1989PRAZOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 072784 · AM THERAP
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.

