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NDC 31722-0596-90

Fenofibrate 145 mg/1 TABLET, FILM COATED

Camber Pharmaceuticals, Inc.

Available — 2-Day Shipping
NDC
31722-0596-90
Generic Name
Fenofibrate
Brand Name
Fenofibrate
Strength
145 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Package Size
—
Labeler
Camber Pharmaceuticals, Inc.

FDA Drug Information

Indications & Usage

1 INDICATIONS AND USAGE Fenofibratetablets are indicated as adjunctive therapy to diet: • to reduce triglyceride (TG) levels in adultswith severe hypertriglyceridemia (TG greater than or equal to 500 mg/dL). • to reduce elevated low-density lipoprotein cholesterol (LDL-C) in adults with primary hyperlipidemia when use of recommended LDL-C lowering therapy is notpossible. Limitations of Use • Markedlyelevated levels of serum TG (e.g. > 2,000 mg/dL) may increase the risk of developing pancreatitis…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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Other Fenofibrate NDC Codes

70756-0215-90160 mg/1TABLET
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27241-0117-03160 mg/1TABLET
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31722-0595-9048 mg/1TABLET, FILM COATED
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70756-0214-9054 mg/1TABLET
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