Pill Identifier Febuxostat - NDC 60687-538
Febuxostat
Product Code 60687-538
Febuxostat by American Health Packaging is a gree rou tablet film coated about 9 mm in size, imprinted with 721. The product is a human prescription drug with active ingredient(s) febuxostat.
Febuxostat
Active Ingredient(s): Febuxostat
Inactive Ingredient(s):
- MICROCRYSTALLINE CELLULOSE
- LACTOSE MONOHYDRATE
- SILICON DIOXIDE
- SODIUM LAURYL SULFATE
- HYDROXYPROPYL CELLULOSE (90000 WAMW)
- CROSCARMELLOSE SODIUM
- MAGNESIUM STEARATE
- POLYVINYL ALCOHOL, UNSPECIFIED
- POLYETHYLENE GLYCOL 3350
- TALC
- TITANIUM DIOXIDE
- D&C YELLOW NO. 10
- FD&C BLUE NO. 1
- FERRIC OXIDE YELLOW
American Health Packaging
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Green (C48329)
Product Packages
NDC Package Code | Package Description |
---|---|
60687-538-21 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-538-11) |
* 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.