Pill Identifier Fenofibrate - NDC 0378-7100
Fenofibrate
Product Code 0378-7100
Fenofibrate by Mylan Pharmaceuticals Inc. is a yellow rou tablet film coated about 9 mm in size, imprinted with klx;170. The product is a human prescription drug with active ingredient(s) fenofibrate.
Fenofibrate
Active Ingredient(s): Fenofibrate
Inactive Ingredient(s):
- BETADEX
- SILICON DIOXIDE
- D&C YELLOW NO. 10
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE
- DOCUSATE SODIUM
- FD&C YELLOW NO. 6
- HYPROMELLOSE, UNSPECIFIED
- MAGNESIUM STEARATE
- MICROCRYSTALLINE CELLULOSE 101
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POLYSORBATE 80
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- TITANIUM DIOXIDE
- SODIUM BENZOATE
- MICROCRYSTALLINE CELLULOSE 102
Mylan Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
0378-7100-77 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
* 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.