Pill Identifier Fenofibrate - NDC 63304-443
Fenofibrate
Product Code 63304-443
Fenofibrate by Sun Pharmaceutical Industries, Inc. is a white capsule about 14 mm in size, imprinted with rg78. The product is a human prescription drug with active ingredient(s) fenofibrate.
Fenofibrate
Active Ingredient(s): Fenofibrate
Inactive Ingredient(s):
- GELATIN, UNSPECIFIED
- HYPROMELLOSE, UNSPECIFIED
- STARCH, CORN
- WATER
- DIMETHICONE
- SILICON DIOXIDE
- SODIUM LAURYL SULFATE
- SODIUM STEARYL FUMARATE
- TALC
- TITANIUM DIOXIDE
- FERROSOFERRIC OXIDE
- POTASSIUM HYDROXIDE
- PROPYLENE GLYCOL
- SHELLAC
- POLYSORBATE 65
- METHYLCELLULOSE (400 MPA.S)
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Capsule
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
63304-443-05 | 500 CAPSULE in 1 BOTTLE |
63304-443-30 | 30 CAPSULE in 1 BOTTLE |
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Pill Identification data last updated on: December, 2018
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product. If this is an emergency, call 911 or the national Poison Help hotline at 1-800-222-1222. Most images are not part of the product labels and have not been verified by the labeler company. ALWAYS consult your physician or pharmacist with any medication-related questions.