NDC 69097-829

Quinapril and Hydrochlorothiazide 20/12.5

Quinapril And Hydrochlorothiazide 20/12.5

Quinapril and Hydrochlorothiazide 20/12.5 is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Cipla Usa Inc.. The primary component is Quinapril Hydrochloride; Hydrochlorothiazide.

Product ID69097-829_4d3f7e7a-ed61-4df6-bc45-f38fb4117406
NDC69097-829
Product TypeHuman Prescription Drug
Proprietary NameQuinapril and Hydrochlorothiazide 20/12.5
Generic NameQuinapril And Hydrochlorothiazide 20/12.5
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-07-20
Marketing CategoryANDA / ANDA
Application NumberANDA201356
Labeler NameCipla USA Inc.
Substance NameQUINAPRIL HYDROCHLORIDE; 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 Through2023-12-31

Packaging

NDC 69097-829-05

90 TABLET in 1 BOTTLE (69097-829-05)
Marketing Start Date2016-07-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69097-829-05 [69097082905]

Quinapril and Hydrochlorothiazide 20/12.5 TABLET
Marketing CategoryANDA
Application NumberANDA201356
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-07-20

Drug Details

Active Ingredients

IngredientStrength
QUINAPRIL HYDROCHLORIDE20 mg/1

OpenFDA Data

SPL SET ID:1de5420c-23d6-40c5-ba24-39143c0f90fb
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310796
  • 310797
  • 310809
  • UPC Code
  • 0369097831059
  • 0369097829056
  • Pharmacological Class

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

    Medicade Reported Pricing

    69097082905 QUINAPRIL-HYDROCHLOROTHIAZIDE 20-12.5 MG TAB

    Pricing Unit: EA | Drug Type:

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