NDC 65862-162

QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE

Quinapril Hydrochloride/hydrochlorothiazide

QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is Quinapril Hydrochloride; Hydrochlorothiazide.

• Product ID: 65862-162_23194091-fa77-4035-b9c1-3120faba7e7e
• NDC: 65862-162
• Product Type: Human Prescription Drug
• Proprietary Name: QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE
• Generic Name: Quinapril Hydrochloride/hydrochlorothiazide
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2007-08-24
• Marketing Category: ANDA / DRUG FOR FURTHER PROCESSING
• Application Number: ANDA078450
• Labeler Name: Aurobindo Pharma Limited
• Substance Name: QUINAPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
• Active Ingredient Strength: 20 mg/1; mg/1
• Pharm Classes: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 65862-162-30

30 TABLET, FILM COATED in 1 BOTTLE (65862-162-30)

• Marketing Start Date: 2007-08-24
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 65862-162-59 [65862016259]

Quinapril Hydrochloride/Hydrochlorothiazide TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078450
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2007-08-24
• Marketing End Date: 2011-08-19

NDC 65862-162-30 [65862016230]

Quinapril Hydrochloride/Hydrochlorothiazide TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078450
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2007-08-24

NDC 65862-162-90 [65862016290]

Quinapril Hydrochloride/Hydrochlorothiazide TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA078450
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2007-08-24

Drug Details

Active Ingredients

Ingredient	Strength
QUINAPRIL HYDROCHLORIDE	20 mg/1

Medicade Reported Pricing

65862016290 QUINAPRIL-HYDROCHLOROTHIAZIDE 20-12.5 MG TAB

Pricing Unit: EA | Drug Type:

65862016230 QUINAPRIL-HYDROCHLOROTHIAZIDE 20-12.5 MG TAB

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE" or generic name "Quinapril Hydrochloride/hydrochlorothiazide"

NDC	Brand Name	Generic Name
35356-998	Quinapril Hydrochloride/Hydrochlorothiazide	Quinapril Hydrochloride/Hydrochlorothiazide
65862-161	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE
65862-162	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE
65862-163	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE