Pill Identifier Fenofibrate - NDC 65862-769
Fenofibrate
Product Code 65862-769
Fenofibrate by Aurobindo Pharma Limited is a white oval tablet coated about 18 mm in size, imprinted with t;16. The product is a human prescription drug with active ingredient(s) fenofibrate.
Fenofibrate
Active Ingredient(s): Fenofibrate
Inactive Ingredient(s):
- CROSPOVIDONE (120 .MU.M)
- HYPROMELLOSE 2910 (3 MPA.S)
- HYPROMELLOSE 2910 (6 MPA.S)
- HYPROMELLOSE 2910 (15 MPA.S)
- MAGNESIUM STEARATE
- MICROCRYSTALLINE CELLULOSE
- POLOXAMER 407
- SILICON DIOXIDE
- SODIUM LAURYL SULFATE
- SUCROSE
- POLYETHYLENE GLYCOL 400
- TITANIUM DIOXIDE
Aurobindo Pharma Limited
Product Type: Human Prescription Drug
Dosage Form: Tablet, Coated
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
65862-769-01 | 100 TABLET, COATED in 1 BOTTLE |
65862-769-05 | 500 TABLET, COATED in 1 BOTTLE |
65862-769-78 | 10 BLISTER PACK in 1 CARTON > 10 TABLET, COATED in 1 BLISTER PACK (65862-769-10) |
65862-769-90 | 90 TABLET, COATED in 1 BOTTLE |
65862-769-99 | 1000 TABLET, COATED 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.