Pill Identifier Fenofibrate - NDC 68788-7578
Fenofibrate
Product Code 68788-7578
Fenofibrate by Preferred Pharmaceuticals, Inc. is a white oval tablet about 18 mm in size, imprinted with fn2. The product is a human prescription drug with active ingredient(s) fenofibrate.
Fenofibrate
Active Ingredient(s): Fenofibrate
Inactive Ingredient(s):
- SILICON DIOXIDE
- CROSCARMELLOSE SODIUM
- CROSPOVIDONE, UNSPECIFIED
- LACTOSE MONOHYDRATE
- EGG PHOSPHOLIPIDS
- MICROCRYSTALLINE CELLULOSE
- POLYVINYL ALCOHOL, UNSPECIFIED
- POVIDONE, UNSPECIFIED
- SODIUM LAURYL SULFATE
- SODIUM STARCH GLYCOLATE TYPE A CORN
- SODIUM STEARYL FUMARATE
- TALC
- TITANIUM DIOXIDE
- XANTHAN GUM
Preferred Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
68788-7578-1 | 100 TABLET in 1 BOTTLE |
68788-7578-3 | 30 TABLET in 1 BOTTLE |
68788-7578-6 | 60 TABLET in 1 BOTTLE |
68788-7578-9 | 90 TABLET in 1 BOTTLE |
* Please review the disclaimer below.
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.