NDC 49999-066

Triamterene and Hydrochlorothiazide

Triamterene And Hydrochlorothiazide

Triamterene and Hydrochlorothiazide is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Lake Erie Medical Dba Quality Care Products Llc. The primary component is Hydrochlorothiazide; Triamterene.

Product ID49999-066_287bedf2-68dc-48df-adf2-0e348415f6ae
NDC49999-066
Product TypeHuman Prescription Drug
Proprietary NameTriamterene and Hydrochlorothiazide
Generic NameTriamterene And Hydrochlorothiazide
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2011-05-04
Marketing CategoryANDA / ANDA
Application NumberANDA074701
Labeler NameLake Erie Medical DBA Quality Care Products LLC
Substance NameHYDROCHLOROTHIAZIDE; TRIAMTERENE
Active Ingredient Strength25 mg/1; mg/1
Pharm ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 49999-066-90

90 CAPSULE in 1 BOTTLE, PLASTIC (49999-066-90)
Marketing Start Date2011-05-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49999-066-30 [49999006630]

Triamterene and Hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA074701
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-05-04
Marketing End Date2014-12-31

NDC 49999-066-60 [49999006660]

Triamterene and Hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA074701
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-05-04
Marketing End Date2014-06-01

NDC 49999-066-00 [49999006600]

Triamterene and Hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA074701
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-05-04
Marketing End Date2014-12-31

NDC 49999-066-90 [49999006690]

Triamterene and Hydrochlorothiazide CAPSULE
Marketing CategoryANDA
Application NumberANDA074701
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-05-04
Marketing End Date2019-10-11

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE25 mg/1

OpenFDA Data

SPL SET ID:e1535638-598a-4d5e-b8e1-31abe65400d2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198316
  • Pharmacological Class

    • Increased Diuresis [PE]
    • Thiazide Diuretic [EPC]
    • Thiazides [CS]
    • Decreased Renal K+ Excretion [PE]
    • Increased Diuresis [PE]
    • Potassium-sparing Diuretic [EPC]