NDC 63304-404

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

Product ID63304-404_02e7b2aa-cc39-461b-b7b1-b0576b7c959e
NDC63304-404
Product TypeHuman Prescription Drug
Proprietary NameFosinopril Sodium and Hydrochlorothiazide
Generic NameFosinopril Sodium And Hydrochlorothiazide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2004-12-20
Marketing CategoryANDA / ANDA
Application NumberANDA076739
Labeler NameRanbaxy 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 FlagE
Listing Certified Through2017-12-31

Packaging

NDC 63304-404-01

10 TABLET in 1 BOTTLE (63304-404-01)
Marketing Start Date2004-12-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63304-404-30 [63304040430]

Fosinopril Sodium and Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA076739
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-12-20
Inactivation Date2019-11-27

NDC 63304-404-01 [63304040401]

Fosinopril Sodium and Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA076739
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-12-20
Inactivation Date2019-11-27

NDC 63304-404-10 [63304040410]

Fosinopril Sodium and Hydrochlorothiazide TABLET
Marketing CategoryANDA
Application NumberANDA076739
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-12-20
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
FOSINOPRIL SODIUM20 mg/1

OpenFDA Data

SPL SET ID:52ee65a7-ca1f-48fd-8fad-d72ea0dad4de
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 857174
  • 857166
    • UPC Code
  • 0363304404012

    • 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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