Pill Identifier Budesonide - NDC 65162-778
Budesonide
Product Code 65162-778
Budesonide by Amneal Pharmaceuticals Llc is a gray and re capsule capsule delayed release about 19 mm in size, imprinted with amneal;778. The product is a human prescription drug with active ingredient(s) budesonide.
Budesonide
Active Ingredient(s): Budesonide
Inactive Ingredient(s):
- CETYL ALCOHOL
- STARCH, CORN
- ETHYLCELLULOSES
- HYPROMELLOSES
- POLYETHYLENE GLYCOLS
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- SODIUM LAURYL SULFATE
- SUCROSE
- TALC
- TRIETHYL CITRATE
- D&C YELLOW NO. 10
- FD&C BLUE NO. 1
- FD&C RED NO. 40
- FD&C YELLOW NO. 6
- GELATIN
- TITANIUM DIOXIDE
- ALCOHOL
- FD&C BLUE NO. 2
- FERROSOFERRIC OXIDE
- METHYL ALCOHOL
- BUTYL ALCOHOL
- PROPYLENE GLYCOL
- SHELLAC
Amneal Pharmaceuticals Llc
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release
- Gray (C48324)
- Red (C48326)
Product Packages
NDC Package Code | Package Description |
---|---|
65162-778-10 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
65162-778-18 | 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
65162-778-30 | 300 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
65162-778-49 | 21 CAPSULE, DELAYED 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.