Pill Identifier Dofetilide - NDC 47335-061
Dofetilide
Product Code 47335-061
Dofetilide by Sun Pharmaceutical Industries, Inc. is a orange and white capsule about 15 mm in size, imprinted with 598;598. The product is a human prescription drug with active ingredient(s) dofetilide.
Dofetilide
Active Ingredient(s): Dofetilide
Inactive Ingredient(s):
- CELLULOSE, MICROCRYSTALLINE
- STARCH, CORN
- MAGNESIUM STEARATE
- GELATIN
- FD&C YELLOW NO. 6
- TITANIUM DIOXIDE
- SHELLAC
- ALCOHOL
- ISOPROPYL ALCOHOL
- BUTYL ALCOHOL
- PROPYLENE GLYCOL
- AMMONIA
- FERROSOFERRIC OXIDE
- POTASSIUM HYDROXIDE
- WATER
- SILICON DIOXIDE
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Capsule
- Orange (C48331)
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
47335-061-79 | 4 BLISTER PACK in 1 CARTON > 10 CAPSULE in 1 BLISTER PACK (47335-061-66) |
47335-061-86 | 60 CAPSULE 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.