Orange Book product · Generic (ANDA)
TAMSULOSIN HYDROCHLORIDE
TAMSULOSIN HYDROCHLORIDE
At a glance
May 04, 2022
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 04, 2022
4 yr 2 mo ago
Today
Pharmaceutical detail
Active ingredient
TAMSULOSIN HYDROCHLORIDE
Strength
0.4MG
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
ANDA 214730
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of TAMSULOSIN HYDROCHLORIDE
- 1997FLOMAXBrand (NDA)
NDA 020579 · SANOFI
- 2025TAMSULOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 219767 · RISING
- 2019TAMSULOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 211885 · CHARTWELL RX
- 2017TAMSULOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 207405 · ALKEM LABS LTD
- 2017TAMSULOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 204645 · MACLEODS PHARMS LTD
- 2013TAMSULOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 202433 · AUROBINDO PHARMA LTD
- 2013TAMSULOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 202010 · PH HEALTH
- 2010TAMSULOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 090931 · SUN PHARM INDS LTD
- 2010TAMSULOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 090408 · PHARMOBEDIENT
- 2010TAMSULOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 078015 · SANDOZ
- 2010TAMSULOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 078938 · SCIEGEN PHARMS
- 2010TAMSULOSIN HYDROCHLORIDEGeneric (ANDA)
ANDA 078801 · SYNTHON BV
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.

