Pill Identifier Duloxetine - NDC 67877-263
Duloxetine
Product Code 67877-263
Duloxetine by Ascend Laboratories, Llc is a gree capsule capsule delayed release about 16 mm in size, imprinted with dulox;20mg. The product is a human prescription drug with active ingredient(s) duloxetine.
Duloxetine
Active Ingredient(s): Duloxetine
Inactive Ingredient(s):
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
- CROSPOVIDONE (120 .MU.M)
- TALC
- TRIETHYL CITRATE
- TITANIUM DIOXIDE
- ISOPROPYL ALCOHOL
- METHYLENE CHLORIDE
- FERRIC OXIDE YELLOW
- FD&C BLUE NO. 2
- GELATIN
- SODIUM LAURYL SULFATE
- HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST)
- HYPROMELLOSE, UNSPECIFIED
- SHELLAC
- BUTYL ALCOHOL
- PROPYLENE GLYCOL
- AMMONIA
- ALCOHOL
- SUCROSE
- POTASSIUM HYDROXIDE
- FERROSOFERRIC OXIDE
Ascend Laboratories, Llc
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release
- Green (C48329)
Product Packages
NDC Package Code | Package Description |
---|---|
67877-263-01 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
67877-263-10 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
67877-263-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
67877-263-60 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
67877-263-90 | 90 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.