Pill Identifier Duloxetine Delayed-release - NDC 50090-3205
Duloxetine Hydrochloride
Product Code 50090-3205
Duloxetine Delayed-release by A-s Medication Solutions is a green and white capsule capsule delayed release pellets about 16 mm in size, imprinted with b;747. The product is a human prescription drug with active ingredient(s) duloxetine hydrochloride.
Duloxetine Delayed-release
Active Ingredient(s): Duloxetine Hydrochloride
Inactive Ingredient(s):
- HYPROMELLOSE, UNSPECIFIED
- TALC
- TITANIUM DIOXIDE
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- SODIUM LAURYL SULFATE
- POLYSORBATE 80
- TRIETHYL CITRATE
- FERROSOFERRIC OXIDE
- PROPYLENE GLYCOL
- AMMONIA
- POTASSIUM HYDROXIDE
- SHELLAC
- SUCROSE
- STARCH, CORN
- GELATIN, UNSPECIFIED
- FD&C BLUE NO. 1
- FD&C YELLOW NO. 6
- D&C YELLOW NO. 10
A-s Medication Solutions
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release Pellets
- Green (C48329)
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
50090-3205-0 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE |
50090-3205-1 | 90 CAPSULE, DELAYED RELEASE 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.