Pill Identifier Budesonide - NDC 68682-309
Budesonide
Product Code 68682-309
Budesonide by Oceanside Pharmaceuticals is a white rou tablet extended release about 10 mm in size, imprinted with mx9. The product is a human prescription drug with active ingredient(s) budesonide.
Budesonide
Active Ingredient(s): Budesonide
Inactive Ingredient(s):
- STEARIC ACID
- LECITHIN, SOYBEAN
- MICROCRYSTALLINE CELLULOSE
- LACTOSE, UNSPECIFIED FORM
- SILICON DIOXIDE
- MAGNESIUM STEARATE
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- TALC
- TRIETHYL CITRATE
- TITANIUM DIOXIDE
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED
Oceanside Pharmaceuticals
Product Type: Human Prescription Drug
Dosage Form: Tablet, Extended Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
68682-309-30 | 30 TABLET, 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.