NDC 23155-061

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 Heritage Pharmaceuticals Inc.. The primary component is Fosinopril Sodium; Hydrochlorothiazide.

Product ID23155-061_199837fb-147b-4251-a0db-08220c0d9045
NDC23155-061
Product TypeHuman Prescription Drug
Proprietary NameFosinopril Sodium and Hydrochlorothiazide
Generic NameFosinopril Sodium And Hydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2011-11-15
Marketing CategoryANDA / ANDA
Application NumberANDA079025
Labeler NameHeritage Pharmaceuticals Inc.
Substance NameFOSINOPRIL SODIUM; HYDROCHLOROTHIAZIDE
Active Ingredient Strength20 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 Through2019-12-31

Packaging

NDC 23155-061-03

30 TABLET in 1 BOTTLE (23155-061-03)
Marketing Start Date2011-11-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 23155-061-05 [23155006105]

Fosinopril Sodium and Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA079025
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-11-15

NDC 23155-061-03 [23155006103]

Fosinopril Sodium and Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA079025
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-11-15

NDC 23155-061-01 [23155006101]

Fosinopril Sodium and Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA079025
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-11-15

Drug Details

Active Ingredients

IngredientStrength
FOSINOPRIL SODIUM20 mg/1

OpenFDA Data

SPL SET ID:9921249f-e15d-46e1-b4ad-4d6866f30ca6
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 857174
  • 857166
    • UPC Code
  • 0323155061031
  • 0323155060034

    • Pharmacological Class

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

    Medicade Reported Pricing

    23155006101 FOSINOPRIL-HYDROCHLOROTHIAZIDE 20-12.5 MG TAB

    Pricing Unit: EA | Drug Type:

    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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