Pill Identifier Budesonide - NDC 0591-2510
Budesonide
Product Code 0591-2510
Budesonide by Actavis Pharma, Inc. is a white rou tablet film coated extended release about 9 mm in size, imprinted with wpi;2510. The product is a human prescription drug with active ingredient(s) budesonide.
Budesonide
Active Ingredient(s): Budesonide
Inactive Ingredient(s):
- SILICON DIOXIDE
- HYDROXYPROPYL CELLULOSE (90000 WAMW)
- HYDROXYPROPYL CELLULOSE (110000 WAMW)
- HYPROMELLOSE 2910 (3 MPA.S)
- HYPROMELLOSE 2910 (6 MPA.S)
- FERROSOFERRIC OXIDE
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:2)
- MICROCRYSTALLINE CELLULOSE
- POLYETHYLENE GLYCOL 400
- POLYSORBATE 80
- PROPYLENE GLYCOL
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- LECITHIN, SOYBEAN
- TALC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
Actavis Pharma, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
0591-2510-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE 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.