Pill Identifier Nabumetone - NDC 0591-3670
Nabumetone
Product Code 0591-3670
Nabumetone by Actavis Pharma, Inc. is a white oval tablet film coated about 17 mm in size, imprinted with 3670. The product is a human prescription drug with active ingredient(s) nabumetone.
Nabumetone
Active Ingredient(s): Nabumetone
Inactive Ingredient(s):
- SILICON DIOXIDE
- STARCH, CORN
- HYPROMELLOSES
- MAGNESIUM STEARATE
- POVIDONE
- SODIUM LAURYL SULFATE
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- TITANIUM DIOXIDE
- TRIACETIN
- TALC
Actavis Pharma, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- White (C48325)
Product Packages
| NDC Package Code | Package Description |
|---|---|
| 0591-3670-00 | 15150 TABLET, FILM COATED in 1 BOX |
| 0591-3670-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 0591-3670-05 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 0591-3670-77 | 18180 TABLET, FILM COATED in 1 CONTAINER |
* 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.