Orange Book product · Brand (NDA)
INDERIDE-40/25
HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
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; PROPRANOLOL HYDROCHLORIDE
Strength
25MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
NDA 018031
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
- 1985INDERIDE LA 120/50Brand (NDA)
NDA 019059 · WYETH AYERST
- 1991PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071498 · WATSON LABS
- 1991PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071501 · WATSON LABS
- 1988PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071552 · IVAX SUB TEVA PHARMS
- 1988PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071553 · IVAX SUB TEVA PHARMS
- 1988PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 072043 · ANI PHARMS
- 1988PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071771 · WARNER CHILCOTT
- 1988PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071772 · WARNER CHILCOTT
- 1987PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071060 · CHARTWELL RX
- 1987PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071061 · CHARTWELL RX
- 1987PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 070947 · RISING
- 1987PROPRANOLOL HYDROCHLORIDE & HYDROCHLOROTHIAZIDEGeneric (ANDA)
ANDA 071126 · DURAMED PHARMS BARR
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.
