SEARCH RESULTS for: Increased Diuresis [Drug Class] (1356 results)

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BUMETANIDE tablet

NDC Code(s): 0615-8393-05, 0615-8393-39, 0615-8394-39
• Packager: NCS HealthCare of KY, LLC dba Vangard Labs
• This is a repackaged label.
• Source NDC Code(s): 69238-1490, 69238-1491

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BUMETANIDE tablet

NDC Code(s): 68071-3128-3, 68071-3128-6, 68071-3128-9
• Packager: NuCare Pharmaceuticals, Inc.
• This is a repackaged label.
• Source NDC Code(s): 42799-120

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BUMETANIDE tablet

NDC Code(s): 54868-3764-0, 54868-3764-1, 54868-3764-2, 54868-3764-3, view more
54868-3765-0, 54868-4352-0, 54868-4352-3, 54868-4352-4, 54868-4352-5
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0185-0128, 0185-0129, 0185-0130

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BUMETANIDE tablet

NDC Code(s): 16571-677-01, 16571-677-10, 16571-678-01, 16571-678-10, view more
16571-679-01
• Packager: Rising Pharma Holdings, Inc

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BUMETANIDE tablet

NDC Code(s): 0185-0128-01, 0185-0128-05, 0185-0129-01, 0185-0129-05, view more
0185-0130-01, 0185-0130-05
• Packager: Sandoz Inc

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BUMETANIDE tablet

NDC Code(s): 51672-4223-1, 51672-4224-1, 51672-4225-1
• Packager: Taro Pharmaceuticals U.S.A., Inc.

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BUMETANIDE tablet

NDC Code(s): 50436-0129-1
• Packager: Unit Dose Services
• This is a repackaged label.
• Source NDC Code(s): 0185-0129

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BUMETANIDE tablet

NDC Code(s): 0832-0540-11, 0832-0541-10, 0832-0541-11, 0832-0542-10, view more
0832-0542-11
• Packager: Upsher-Smith Laboratories, LLC

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BUMETANIDE tablet

NDC Code(s): 70771-1024-0, 70771-1024-1, 70771-1024-3, 70771-1024-5, view more
70771-1024-9, 70771-1025-0, 70771-1025-1, 70771-1025-3, 70771-1025-5, 70771-1025-9, 70771-1026-0, 70771-1026-1, 70771-1026-3, 70771-1026-5, 70771-1026-9
• Packager: Zydus Lifesciences Limited

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BUMETANIDE tablet

NDC Code(s): 68382-525-01, 68382-525-05, 68382-525-06, 68382-525-10, view more
68382-525-16, 68382-526-01, 68382-526-05, 68382-526-06, 68382-526-10, 68382-526-16, 68382-527-01, 68382-527-05, 68382-527-06, 68382-527-10, 68382-527-16
• Packager: Zydus Pharmaceuticals (USA) Inc.

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BUMEX (bumetanide) tablet

NDC Code(s): 30698-630-01, 30698-631-01, 30698-632-01
• Packager: Validus Pharmaceuticals LLC

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CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 62559-660-90, 62559-661-90, 62559-662-90
• Packager: ANI Pharmaceuticals, Inc.

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CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 33342-131-10, 33342-131-12, 33342-131-15, 33342-131-51, view more
33342-132-10, 33342-132-12, 33342-132-15, 33342-132-51, 33342-133-10, 33342-133-12, 33342-133-15, 33342-133-51
• Packager: Macleods Pharmaceuticals Limited

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CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 0378-3001-05, 0378-3001-77, 0378-3002-05, 0378-3002-77, view more
0378-3003-05, 0378-3003-77
• Packager: Mylan Pharmaceuticals Inc.

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CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 43547-459-09, 43547-459-50, 43547-460-09, 43547-460-50, view more
43547-461-09, 43547-461-50
• Packager: Solco Healthcare LLC

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CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 70771-1325-0, 70771-1325-1, 70771-1325-2, 70771-1325-3, view more
70771-1325-4, 70771-1325-9, 70771-1326-0, 70771-1326-1, 70771-1326-2, 70771-1326-3, 70771-1326-4, 70771-1326-9, 70771-1327-0, 70771-1327-1, 70771-1327-2, 70771-1327-3, 70771-1327-4, 70771-1327-9
• Packager: Zydus Lifesciences Limited

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CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 68382-194-01, 68382-194-06, 68382-194-10, 68382-194-16, view more
68382-194-77, 68382-195-01, 68382-195-06, 68382-195-10, 68382-195-16, 68382-195-77, 68382-416-01, 68382-416-06, 68382-416-10, 68382-416-16, 68382-416-77
• Packager: Zydus Pharmaceuticals USA Inc.

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CAPTOPRIL AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 54868-4062-0, 54868-4062-1, 54868-5787-0
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0378-0083, 0378-0086

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CAPTOPRIL AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 16571-827-09, 16571-828-09, 16571-829-09, 16571-830-09
• Packager: Rising Pharma Holdings, Inc.

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CHLOROTHIAZIDE (chlorothiazide sodium) injection, powder, lyophilized, for solution

NDC Code(s): 63323-658-94
• Packager: Fresenius Kabi USA, LLC