Quinapril And Hydrochlorothiazide Tablet
NDC 62135-668
Product Information
Quinapril And Hydrochlorothiazide is a ANDA-approved product labeled by Chartwell Rx, Llc. This medication is typically used as a angiotensin converting enzyme inhibitor [epc]. It is supplied as a orange tablet for oral administration. This product entry covers the primary NDC 62135-668 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
Clinical Specifications
Labeler & Regulatory Data
Marketing Timeline
Product Characteristics
11 MM
CE;153
CE;154
Code Structure Chart
Product Details
What is NDC 62135-668?
What are the uses of this product?
What are Active Ingredients of this product?
- HYDROCHLOROTHIAZIDE 12.5 mg/1 - A thiazide diuretic often considered the prototypical member of this class. It reduces the reabsorption of electrolytes from the renal tubules. This results in increased excretion of water and electrolytes, including sodium, potassium, chloride, and magnesium. It is used in the treatment of several disorders including edema, hypertension, diabetes insipidus, and hypoparathyroidism.
- QUINAPRIL HYDROCHLORIDE 20 mg/1 - A tetrahydroisoquinoline derivative and ANGIOTENSIN CONVERTING ENZYME inhibitor that is used in the treatment of HYPERTENSION and HEART FAILURE.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- QUINAPRIL HYDROCHLORIDE (UNII: 33067B3N2M)
- QUINAPRILAT (UNII: 34SSX5LDE5) (Active Moiety)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (Active Moiety)
Which are the Inactive Ingredients associated UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE 101 (UNII: 7T9FYH5QMK)
- CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TALC (UNII: 7SEV7J4R1U)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MICROCRYSTALLINE CELLULOSE 102 (UNII: PNR0YF693Y)
What is the NDC to RxNorm Crosswalk for this product?
- RxCUI: 310796 - quinapril 10 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
- RxCUI: 310796 - hydrochlorothiazide 12.5 MG / quinapril 10 MG Oral Tablet
- RxCUI: 310796 - HCTZ 12.5 MG / quinapril (as quinapril hydrochloride) 10 MG Oral Tablet
- RxCUI: 310796 - HCTZ 12.5 MG / quinapril 10 MG Oral Tablet
- RxCUI: 310797 - quinapril 20 MG / hydroCHLOROthiazide 12.5 MG Oral Tablet
Which are the Pharmacologic Classes of this product?
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