Pill Identifier Fenofibric Acid - NDC 46708-244
Fenofibric Acid
Product Code 46708-244
Fenofibric Acid by Alembic Pharmaceuticals Limited is a brow capsule capsule delayed release about 16 mm in size, imprinted with a;138. The product is a human prescription drug with active ingredient(s) fenofibric acid.
Fenofibric Acid
Active Ingredient(s): Fenofibric Acid
Inactive Ingredient(s):
- HYPROMELLOSES
- POVIDONE K30
- WATER
- HYDROXYPROPYL CELLULOSE (TYPE E)
- SILICON DIOXIDE
- SODIUM STEARYL FUMARATE
- METHACRYLIC ACID
- TALC
- TRIETHYL CITRATE
- GELATIN
- TITANIUM DIOXIDE
- FERRIC OXIDE YELLOW
- FERRIC OXIDE RED
- SHELLAC
- PROPYLENE GLYCOL
- POTASSIUM HYDROXIDE
- FERROSOFERRIC OXIDE
Alembic Pharmaceuticals Limited
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release
- Brown (C48332)
Product Packages
NDC Package Code | Package Description |
---|---|
46708-244-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
46708-244-90 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
46708-244-91 | 1000 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.