SEARCH RESULTS for: 854916 [RxCUI] (18 results)

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 10544-173-30, 10544-174-90, 10544-563-30
• Packager: Blenheim Pharmacal, Inc.
• This is a repackaged label.
• Source NDC Code(s): 29300-187, 29300-188, 29300-189

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 71335-1161-1, 71335-1161-2, 71335-1161-3
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 29300-187

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet, coated

NDC Code(s): 54868-4576-0, 54868-4576-1, 54868-4576-2, 54868-4576-3, view more
54868-4577-0, 54868-4577-1, 54868-4577-2, 54868-4577-3, 54868-4578-0, 54868-4578-1, 54868-4578-2, 54868-4578-3
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0185-0701, 0185-0704, 0185-0707

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 50090-6478-0
• Packager: A-S Medication Solutions
• This is a repackaged label.
• Source NDC Code(s): 0093-3241

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 71335-1931-1, 71335-1931-2, 71335-1931-3
• Packager: Bryant Ranch Prepack
• This is a repackaged label.
• Source NDC Code(s): 42799-920

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 42799-920-01, 42799-920-02, 42799-920-30, 42799-921-01, view more
42799-921-02, 42799-921-30, 42799-922-01, 42799-922-02, 42799-922-30
• Packager: Edenbridge Pharmaceuticals LLC.

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 68462-878-01, 68462-878-05, 68462-878-30, 68462-879-01, view more
68462-879-05, 68462-879-30, 68462-880-01, 68462-880-05, 68462-880-30
• Packager: GLENMARK PHARMACEUTICALS INC., USA

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 0378-0501-01, 0378-0501-05, 0378-0503-01, 0378-0503-05, view more
0378-0505-01, 0378-0505-05
• Packager: Mylan Pharmaceuticals Inc.

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 70518-3333-0
• Packager: REMEDYREPACK INC.
• This is a repackaged label.
• Source NDC Code(s): 0378-0501

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 0093-3241-01, 0093-3242-01, 0093-3243-56
• Packager: Teva Pharmaceuticals USA, Inc.

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 72578-113-01, 72578-113-05, 72578-113-06, 72578-114-01, view more
72578-114-05, 72578-114-06, 72578-115-01, 72578-115-05, 72578-115-06
• Packager: Viona Pharmaceuticals Inc

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet, film coated

NDC Code(s): 70771-1760-1, 70771-1760-3, 70771-1760-5, 70771-1761-1, view more
70771-1761-3, 70771-1761-5, 70771-1762-1, 70771-1762-3, 70771-1762-5
• Packager: Zydus Lifesciences Limited

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 10135-740-01, 10135-740-05, 10135-741-01, 10135-741-05, view more
10135-742-05, 10135-742-30
• Packager: Marlex Pharmaceuticals, Inc.
• This is a repackaged label.
• Source NDC Code(s): 70954-412, 70954-413, 70954-414

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 70954-412-10, 70954-412-30, 70954-412-40, 70954-413-10, view more
70954-413-30, 70954-413-40, 70954-414-10, 70954-414-30, 70954-414-40
• Packager: Novitium Pharma LLC

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 67296-1268-3
• Packager: RedPharm Drug, Inc.
• This is a repackaged label.
• Source NDC Code(s): 29300-187

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BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE tablet

NDC Code(s): 29300-187-01, 29300-187-05, 29300-187-10, 29300-187-13, view more
29300-188-01, 29300-188-05, 29300-188-10, 29300-188-13, 29300-189-01, 29300-189-05, 29300-189-10, 29300-189-13
• Packager: Unichem Pharmaceuticals (USA), Inc.

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bisoprolol fumarate hydrochlorothiazide (Bisoprolol Fumarate and hydrochlorothiazide) tablet, film coated

NDC Code(s): 0591-0841-01, 0591-0841-05, 0591-0842-01, 0591-0842-05, view more
0591-0843-01, 0591-0843-30
• Packager: Watson Laboratories, Inc.

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ZIAC (bisoprolol fumarate and hydrochlorothiazide) tablet, film coated

NDC Code(s): 51285-040-01, 51285-047-02, 51285-050-02
• Packager: Teva Women's Health LLC