Pill Identifier Fenofibric Acid Delayed-release - NDC 24979-109
Fenofibric Acid
Product Code 24979-109
Fenofibric Acid Delayed-release by Twi Pharmaceuticals, Inc. is a yellow and brow capsule capsule delayed release about 16 mm in size, imprinted with twi;t109;45mg. 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):
- HYDROXYPROPYL CELLULOSE (TYPE M)
- HYPROMELLOSE 2208 (4000 MPA.S)
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- silicon dioxide
- TALC
- TRIETHYL CITRATE
- FERROSOFERRIC OXIDE
- GELATIN
- SODIUM LAURYL SULFATE
- SHELLAC
- PROPYLENE GLYCOL
- FERRIC OXIDE RED
- TITANIUM DIOXIDE
- FERRIC OXIDE YELLOW
- AMMONIA
Twi Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release
- Yellow (C48330)
- Brown (C48332)
Product Packages
NDC Package Code | Package Description |
---|---|
24979-109-07 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
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Pill Identification data last updated on: December, 2018
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