Pill Identifier Fenofibrate - NDC 42385-935
Fenofibrate
Product Code 42385-935
Fenofibrate by Laurus Labs Limited is a yellow rou tablet film coated about 9 mm in size, imprinted with 201. The product is a human prescription drug with active ingredient(s) fenofibrate.
Fenofibrate
Active Ingredient(s): Fenofibrate
Inactive Ingredient(s):
- CELLULOSE, MICROCRYSTALLINE
- CROSPOVIDONE, UNSPECIFIED
- D&C YELLOW NO. 10
- FD&C BLUE NO. 2
- FD&C YELLOW NO. 6
- LACTOSE MONOHYDRATE
- LECITHIN, SOYBEAN
- POLYVINYL ALCOHOL, UNSPECIFIED
- POVIDONE K30
- SILICON DIOXIDE
- SODIUM LAURYL SULFATE
- SODIUM STEARYL FUMARATE
- TALC
- TITANIUM DIOXIDE
- XANTHAN GUM
Laurus Labs Limited
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
42385-935-05 | 500 TABLET, FILM COATED in 1 BOTTLE |
42385-935-11 | 1000 TABLET, FILM COATED in 1 BOTTLE |
42385-935-30 | 30 TABLET, FILM COATED in 1 BOTTLE |
42385-935-90 | 90 TABLET, FILM COATED 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.