Pill Identifier Fenofibric Acid - NDC 42571-347
Fenofibric Acid
Product Code 42571-347
Fenofibric Acid by Micro Labs Limited is a red and yellow capsule capsule delayed release about 16 mm in size, imprinted with cdr;45. The product is a human prescription drug with active ingredient(s) fenofibric acid.
Fenofibric Acid
Active Ingredient(s): Fenofibric Acid
Inactive Ingredient(s):
- HYPROMELLOSE 2208 (15000 MPA.S)
- HYDROXYPROPYL CELLULOSE (110000 WAMW)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- MICROCRYSTALLINE CELLULOSE 101
- POVIDONE K30
- SILICON DIOXIDE
- SODIUM STEARYL FUMARATE
- TALC
- TRIETHYL CITRATE
- FERROSOFERRIC OXIDE
- FERRIC OXIDE RED
- GELATIN
- TITANIUM DIOXIDE
Micro Labs Limited
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release
- Red (C48326)
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
42571-347-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
42571-347-90 | 90 CAPSULE, DELAYED RELEASE 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.