Pill Identifier Fenofibric Acid Delayed-release - NDC 69844-023
Fenofibric Acid
Product Code 69844-023
Fenofibric Acid Delayed-release by Graviti Pharmaceuticals Private Limited is a blue capsule capsule delayed release about 22 mm in size, imprinted with 168. The product is a human prescription drug with active ingredient(s) fenofibric acid.
Fenofibric Acid Delayed-release
Active Ingredient(s): Fenofibric Acid
Inactive Ingredient(s):
- AMMONIA
- FD&C BLUE NO. 1
- FD&C RED NO. 3
- FD&C RED NO. 40
- FERRIC OXIDE YELLOW
- FERROSOFERRIC OXIDE
- GELATIN
- HYDROXYPROPYL CELLULOSE (90000 WAMW)
- HYPROMELLOSE 2208 (15000 MPA.S)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- POLYSORBATE 80
- POTASSIUM HYDROXIDE
- POVIDONE K30
- PROPYLENE GLYCOL
- SHELLAC
- SILICON DIOXIDE
- SODIUM LAURYL SULFATE
- SODIUM STEARYL FUMARATE
- TALC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
Graviti Pharmaceuticals Private Limited
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release
- Blue (C48333)
Product Packages
NDC Package Code | Package Description |
---|---|
69844-023-01 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
69844-023-02 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
69844-023-03 | 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.