SEARCH RESULTS for: Peroxisome Proliferator-activated Receptor alpha Agonists [Drug Class] (186 results)

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ACTOPLUS MET (pioglitazone and metformin hydrochloride) tablet, film coated

NDC Code(s): 64764-158-18, 64764-158-41, 64764-158-60
• Packager: Takeda Pharmaceuticals America, Inc.

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ACTOPLUS MET (pioglitazone hydrochloride and metformin hydrochloride) tablet, film coated

NDC Code(s): 54868-5500-0, 54868-5500-1, 54868-5500-2, 54868-5553-0, view more
54868-5553-1, 54868-5553-2
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 64764-155, 64764-158

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ACTOS (pioglitazone hydrochloride) tablet

NDC Code(s): 68258-3034-3, 68258-5230-3
• Packager: Dispensing Solutions, Inc.
• This is a repackaged label.
• Source NDC Code(s): 64764-151, 64764-301

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ACTOS (pioglitazone hydrochloride) tablet

NDC Code(s): 54868-4343-0, 54868-4354-0, 54868-4354-1, 54868-4391-0, view more
54868-4391-1
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 64764-151, 64764-301, 64764-451

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ACTOS (pioglitazone hydrochloride) tablet

NDC Code(s): 21695-147-15, 21695-148-15
• Packager: Rebel Distributors Corp.
• This is a repackaged label.
• Source NDC Code(s): 64764-151, 64764-0301

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ACTOS (pioglitazone) tablet

NDC Code(s): 64764-151-02, 64764-151-04, 64764-151-05, 64764-151-06, view more
64764-301-02, 64764-301-14, 64764-301-15, 64764-301-16, 64764-451-02, 64764-451-24, 64764-451-25, 64764-451-26
• Packager: Takeda Pharmaceuticals America, Inc.

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ALOGLIPTIN AND PIOGLITAZONE (alogliptin benzoate and pioglitazone hydrochloride) tablet, film coated

NDC Code(s): 45802-260-65, 45802-351-65, 45802-402-65, 45802-499-65
• Packager: Padagis Israel Pharmaceuticals Ltd

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antara (fenofibrate) capsule

NDC Code(s): 67707-043-30, 67707-043-99, 67707-130-30, 67707-130-99
• Packager: Oscient Pharmaceuticals Corporation

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DUETACT (pioglitazone and glimepiride) tablet

NDC Code(s): 64764-302-30, 64764-302-90, 64764-304-30, 64764-304-90
• Packager: Takeda Pharmaceuticals America, Inc.

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FENOFIBRATE capsule

NDC Code(s): 54868-5575-0, 54868-5575-1, 54868-5575-2, 54868-5994-0, view more
54868-5994-1
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0115-0522, 0115-0533

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FENOFIBRATE tablet

NDC Code(s): 33261-966-30
• Packager: Aidarex Pharmaceuticals LLC
• This is a repackaged label.
• Source NDC Code(s): 0115-5511

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FENOFIBRATE tablet, film coated

NDC Code(s): 61919-831-30
• Packager: DirectRX
• This is a repackaged label.
• Source NDC Code(s): 63304-901

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FENOFIBRATE tablet, film coated

NDC Code(s): 51655-901-52
• Packager: Northwind Pharmaceuticals, LLC
• This is a repackaged label.
• Source NDC Code(s): 63304-901

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FENOFIBRATE tablet

NDC Code(s): 51655-010-52
• Packager: Northwind Pharmaceuticals
• This is a repackaged label.
• Source NDC Code(s): 0093-2060

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FENOFIBRATE tablet

NDC Code(s): 51655-902-52
• Packager: NORTHWIND PHARMACEUTICALS
• This is a repackaged label.
• Source NDC Code(s): 68382-230

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FENOFIBRATE tablet

NDC Code(s): 54868-5660-0, 54868-5660-1, 54868-5697-0, 54868-5697-1
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 0115-5511, 0115-5522

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FENOGLIDE (fenofibrate) tablet

NDC Code(s): 54868-6118-0
• Packager: Physicians Total Care, Inc.
• This is a repackaged label.
• Source NDC Code(s): 59630-495

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FENOGLIDE (fenofibrate) tablet

NDC Code(s): 52725-490-90, 52725-495-07, 52725-495-90
• Packager: Shore Therapeutics, Inc

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gemfibrozil (Gemfibrozil) tablet

NDC Code(s): 0591-0454-05, 0591-0454-60
• Packager: Watson Laboratories, Inc.

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GEMFIBROZIL tablet

NDC Code(s): 53217-251-30, 53217-251-60, 53217-251-90, 53217-251-99
• Packager: Aidarex Pharmaceuticals LLC
• This is a repackaged label.
• Source NDC Code(s): 69097-821