Pill Identifier Budesonide - NDC 16714-829
Budesonide
Product Code 16714-829
Budesonide by Northstar Rx Llc. is a orange and white capsule capsule coated pellets about 19 mm in size, imprinted with 720. The product is a human prescription drug with active ingredient(s) budesonide.
Budesonide
Active Ingredient(s): Budesonide
Inactive Ingredient(s):
- ACETYLTRIBUTYL CITRATE
- ALCOHOL
- AMMONIA
- BUTYL ALCOHOL
- DIMETHICONE
- ETHYLCELLULOSES
- FERRIC OXIDE RED
- FERRIC OXIDE YELLOW
- FERROSOFERRIC OXIDE
- GELATIN
- ISOPROPYL ALCOHOL
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- POLYSORBATE 80
- POTASSIUM HYDROXIDE
- PROPYLENE GLYCOL
- SHELLAC
- SODIUM LAURYL SULFATE
- SUCROSE
- TALC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
- WATER
Northstar Rx Llc.
Product Type: Human Prescription Drug
Dosage Form: Capsule, Coated Pellets
- Orange (C48331)
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
16714-829-01 | 100 CAPSULE, COATED PELLETS 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.