NDC 63629-6993

Fosinopril Sodium and Hydrochlorothiazide

Fosinopril Sodium And Hydrochlorothiazide

Fosinopril Sodium and Hydrochlorothiazide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Fosinopril Sodium; Hydrochlorothiazide.

Product ID63629-6993_2c585e38-3944-48bc-9a4f-a1da892a9342
NDC63629-6993
Product TypeHuman Prescription Drug
Proprietary NameFosinopril Sodium and Hydrochlorothiazide
Generic NameFosinopril Sodium And Hydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-07-09
Marketing CategoryANDA / ANDA
Application NumberANDA079245
Labeler NameBryant Ranch Prepack
Substance NameFOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Active Ingredient Strength10 mg/1; mg/1
Pharm ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 63629-6993-1

30 TABLET in 1 BOTTLE (63629-6993-1)
Marketing Start Date2016-04-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-6993-1 [63629699301]

Fosinopril Sodium and Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA079245
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-04-29
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
FOSINOPRIL SODIUM10 mg/1

OpenFDA Data

SPL SET ID:ebbddf45-1664-4815-bf26-1639a26bc894
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 857166

    • Pharmacological Class

    • Angiotensin Converting Enzyme Inhibitor [EPC]
    • Angiotensin-converting Enzyme Inhibitors [MoA]
    • Increased Diuresis [PE]
    • Thiazide Diuretic [EPC]
    • Thiazides [CS]

    NDC Crossover Matching brand name "Fosinopril Sodium and Hydrochlorothiazide" or generic name "Fosinopril Sodium And Hydrochlorothiazide"

    NDCBrand NameGeneric Name
    23155-060Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide Tablet
    23155-061Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
    57237-026Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
    57237-027Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
    63304-403Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
    63304-404Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
    63629-6993Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
    65862-308Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
    65862-309Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
    68462-554Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
    68462-555Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
    69097-972Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
    69097-973Fosinopril Sodium and HydrochlorothiazideFosinopril Sodium and Hydrochlorothiazide
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