SEARCH RESULTS for: Angiotensin 2 Receptor Blocker [Drug Class] (818 results)

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ATACAND (candesartan cilexetil) tablet

NDC Code(s): 68151-4146-3
• Packager: Carilion Materials Management
• This is a repackaged label.
• Source NDC Code(s): 0186-0008

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ATACAND (candesartan cilexetil) tablet

NDC Code(s): 54868-4413-0, 54868-4612-0, 54868-5489-0, 54868-5591-0
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0186-0004, 0186-0008, 0186-0016, 0186-0032

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ATACAND HCT (candesartan cilexetil and hydrochlorothiazide) tablet

NDC Code(s): 62559-650-90, 62559-651-90, 62559-652-90
• Packager: ANI Pharmaceuticals, Inc.

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ATACAND HCT (candesartan cilexetil and hydrochlorothiazide) tablet

NDC Code(s): 54868-4729-0, 54868-4869-0
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0186-0162, 0186-0322

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AVALIDE (irbesartan and hydrochlorothiazide) tablet
AVALIDE (irbesartan and hydrochlorothiazide) tablet, film coated

NDC Code(s): 54868-4494-0, 54868-4526-0, 54868-4526-1, 54868-5465-0, view more
54868-5465-1
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0087-2775, 0087-2776, 0087-2788

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AVALIDE (irbesartan and hydrochlorothiazide) tablet, film coated

NDC Code(s): 0024-5855-30, 0024-5855-90, 0024-5856-30, 0024-5856-90
• Packager: sanofi-aventis U.S. LLC

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AVAPRO (irbesartan) tablet, film coated

NDC Code(s): 0024-5850-30, 0024-5850-90, 0024-5851-30, 0024-5851-90, view more
0024-5852-30, 0024-5852-90
• Packager: Sanofi-Aventis U.S. LLC

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AVAPRO (irbesartan) tablet

NDC Code(s): 35356-854-30
• Packager: Lake Erie Medical DBA Quality Care Products LLC
• This is a repackaged label.
• Source NDC Code(s): 0024-5851

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AVAPRO (irbesartan) tablet

NDC Code(s): 54868-4199-0, 54868-4199-1, 54868-4199-2, 54868-4414-0, view more
54868-4414-1
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0087-2772, 0087-2773

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AX PHARMACEUTICAL CORP (losartan potassium) powder

NDC Code(s): 62157-453-01
• Packager: AX Pharmaceutical Corp

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AX PHARMACEUTICAL CORP (losartan potassium) powder

NDC Code(s): 62157-452-01
• Packager: AX Pharmaceutical Corp

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AX PHARMACEUTICAL CORP (telmisartan) powder

NDC Code(s): 62157-522-01
• Packager: AX Pharmaceutical Corp

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AZOR (amlodipine besylate and olmesartan medoxomil) tablet, film coated

NDC Code(s): 0713-0870-30, 0713-0871-30, 0713-0872-30, 0713-0873-30
• Packager: Cosette Pharmaceuticals, Inc.

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AZOR (amlodipine besylate and olmesartan medoxomil) tablet, film coated

NDC Code(s): 65597-110-07, 65597-110-10, 65597-110-11, 65597-110-30, view more
65597-110-90, 65597-111-07, 65597-111-10, 65597-111-11, 65597-111-30, 65597-111-90, 65597-112-07, 65597-112-10, 65597-112-11, 65597-112-30, 65597-112-90, 65597-113-07, 65597-113-10, 65597-113-11, 65597-113-30, 65597-113-90
• Packager: Daiichi Sankyo Inc.

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AZOR (amlodipine besylate and olmesartan medoxomil) tablet, film coated

NDC Code(s): 54868-6036-0, 54868-6250-0
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 65597-110, 65597-113

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BENICAR HCT (olmesartan medoxomil and hydrochlorothiazide) tablet, film coated

NDC Code(s): 54868-5075-0, 54868-5075-1, 54868-5078-0, 54868-5078-1, view more
54868-5170-0, 54868-5170-1
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 65597-105, 65597-106, 65597-107

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BENICAR HCT (olmesartan medoxomil-hydrochlorothiazide) tablet, film coated

NDC Code(s): 0713-0863-30, 0713-0864-30, 0713-0865-30
• Packager: Cosette Pharmaceuticals, Inc.

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BENICAR (olmesartan medoxomil) tablet, film coated

NDC Code(s): 68151-4633-3
• Packager: Carilion Materials Management
• This is a repackaged label.
• Source NDC Code(s): 65597-101

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BENICAR (olmesartan medoxomil) tablet, film coated

NDC Code(s): 0713-0860-30, 0713-0861-30, 0713-0862-30
• Packager: Cosette Pharmaceuticals, Inc.

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BENICAR (olmesartan medoxomil) tablet, film coated

NDC Code(s): 51138-211-30, 51138-212-30, 51138-213-30
• Packager: Med-Health Pharma, LLC
• This is a repackaged label.
• Source NDC Code(s): 65597-101, 65597-103, 65597-104