NDC 63304-161

Quinapril Hydrochloride and Hydrochlorothiazide

Quinapril Hydrochloride And Hydrochlorothiazide

Quinapril Hydrochloride and Hydrochlorothiazide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Ranbaxy Pharmaceuticals Inc.. The primary component is Hydrochlorothiazide; Quinapril Hydrochloride.

Product ID63304-161_91baf595-84c1-47db-89b2-e6590d282dec
NDC63304-161
Product TypeHuman Prescription Drug
Proprietary NameQuinapril Hydrochloride and Hydrochlorothiazide
Generic NameQuinapril Hydrochloride And Hydrochlorothiazide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2009-03-04
Marketing CategoryANDA / ANDA
Application NumberANDA078211
Labeler NameRanbaxy Pharmaceuticals Inc.
Substance NameHYDROCHLOROTHIAZIDE; QUINAPRIL HYDROCHLORIDE
Active Ingredient Strength13 mg/1; mg/1
Pharm ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 63304-161-30

30 TABLET, FILM COATED in 1 BOTTLE (63304-161-30)
Marketing Start Date2009-03-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63304-161-30 [63304016130]

Quinapril Hydrochloride and Hydrochlorothiazide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078211
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-03-04
Inactivation Date2020-01-31

NDC 63304-161-10 [63304016110]

Quinapril Hydrochloride and Hydrochlorothiazide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078211
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-03-04
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
HYDROCHLOROTHIAZIDE12.5 mg/1

OpenFDA Data

SPL SET ID:b630824c-bee7-4a78-9349-d995c1eb0f16
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310796
  • 310797
  • 310809

    • Pharmacological Class

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

    NDC Crossover Matching brand name "Quinapril Hydrochloride and Hydrochlorothiazide" or generic name "Quinapril Hydrochloride And Hydrochlorothiazide"

    NDCBrand NameGeneric Name
    31722-374Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    31722-375Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    31722-376Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    59762-0220quinapril hydrochloride and hydrochlorothiazidequinapril hydrochloride and hydrochlorothiazide
    59762-0222quinapril hydrochloride and hydrochlorothiazidequinapril hydrochloride and hydrochlorothiazide
    59762-0223quinapril hydrochloride and hydrochlorothiazidequinapril hydrochloride and hydrochlorothiazide
    60505-3409Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    60505-3410Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    60505-3411Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    63304-161Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    63304-162Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    63304-163Quinapril Hydrochloride and HydrochlorothiazideQuinapril Hydrochloride and Hydrochlorothiazide
    0071-0220ACCURETICquinapril hydrochloride and hydrochlorothiazide
    0071-0222ACCURETICquinapril hydrochloride and hydrochlorothiazide
    0071-0223ACCURETICquinapril hydrochloride and hydrochlorothiazide
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.