Orange Book product · Generic (ANDA)
TELMISARTAN AND HYDROCHLOROTHIAZIDE
HYDROCHLOROTHIAZIDE; TELMISARTAN
At a glance
Feb 25, 2014
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 25, 2014
12 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
HYDROCHLOROTHIAZIDE; TELMISARTAN
Strength
12.5MG;40MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 091648
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of HYDROCHLOROTHIAZIDE; TELMISARTAN
- 2000MICARDIS HCTBrand (NDA)
NDA 021162 · BOEHRINGER INGELHEIM
- 2025TELMISARTAN AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 218406 · MANKIND PHARMA
- 2019TELMISARTAN AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 202544 · GLENMARK PHARMS LTD
- 2017TELMISARTAN AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 209028 · PRINSTON INC
- 2017TELMISARTAN AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 204221 · ZYDUS PHARMS
- 2016TELMISARTAN AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 208727 · AUROBINDO PHARMA
- 2015TELMISARTAN AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 204169 · MACLEODS PHARMS LTD
- 2014TELMISARTAN AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 091351 · LUPIN
- 2014TELMISARTAN AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 203010 · ALEMBIC
- 2014TELMISARTAN AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 201192 · TORRENT
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.
