Orange Book product · Brand (NDA)
ALDORIL 15
HYDROCHLOROTHIAZIDE; METHYLDOPA
At a glance
Approved Prior to Jan 1, 1982
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
HYDROCHLOROTHIAZIDE; METHYLDOPA
Strength
15MG;250MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
NDA 013402
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.
- 1989METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 072507 · DAVA PHARMS INC
- 1989METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 072508 · DAVA PHARMS INC
- 1989METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 072509 · DAVA PHARMS INC
- 1989METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 072510 · DAVA PHARMS INC
- 1989METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 070958 · WATSON LABS
- 1989METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 070960 · WATSON LABS
- 1989METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 070959 · WATSON LABS
- 1989METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071069 · WATSON LABS
- 1988METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071920 · WATSON LABS
- 1988METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071921 · WATSON LABS
- 1988METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071922 · WATSON LABS
- 1988METHYLDOPA AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071923 · WATSON LABS
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.
