Pill Identifier Fenofibric Acid - NDC 68180-129
Fenofibric Acid
Product Code 68180-129
Fenofibric Acid by Lupin Pharmaceuticals, Inc. is a blue and yellow capsule capsule delayed release about 21 mm in size, imprinted with lu;q42. The product is a human prescription drug with active ingredient(s) fenofibric acid.
Fenofibric Acid
Active Ingredient(s): Fenofibric Acid
Inactive Ingredient(s):
- DIBUTYL SEBACATE
- ETHYLCELLULOSES
- FD&C BLUE NO. 1
- FERRIC OXIDE YELLOW
- FERROSOFERRIC OXIDE
- GELATIN
- HYPROMELLOSES
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- POTASSIUM HYDROXIDE
- POVIDONE K90
- PROPYLENE GLYCOL
- SHELLAC
- SILICON DIOXIDE
- SODIUM LAURYL SULFATE
- SODIUM STEARYL FUMARATE
- TALC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
Lupin Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release
- Blue (C48333)
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
68180-129-01 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
68180-129-02 | 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
68180-129-09 | 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.