Pill Identifier Duloxetine Hydrochloride - NDC 33342-162
Duloxetine Hydrochloride
Product Code 33342-162
Duloxetine Hydrochloride by Macleods Pharmaceuticals Limited is a blue and gree capsule capsule delayed release about 20 mm in size, imprinted with c81. The product is a human prescription drug with active ingredient(s) duloxetine hydrochloride.
Duloxetine Hydrochloride
Active Ingredient(s): Duloxetine Hydrochloride
Inactive Ingredient(s):
- FD&C BLUE NO. 2
- GELATIN
- HYPROMELLOSES
- SODIUM LAURYL SULFATE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- SUCROSE
- TALC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
- FERRIC OXIDE YELLOW
- STARCH, CORN
Macleods Pharmaceuticals Limited
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release
- Blue (C48333)
- Green (C48329)
Product Packages
NDC Package Code | Package Description |
---|---|
33342-162-07 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
33342-162-10 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
33342-162-12 | 10 BLISTER PACK in 1 CARTON > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
33342-162-44 | 1000 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.