Pill Identifier Diclofenac Sodium Delayed Release - NDC 70934-165
Diclofenac Sodium
Product Code 70934-165
Diclofenac Sodium Delayed Release by Denton Pharma, Inc. Dba Northwind Pharmaceuticals is a white rou tablet delayed release about 10 mm in size, imprinted with cti;103. The product is a human prescription drug with active ingredient(s) diclofenac sodium.
Diclofenac Sodium Delayed Release
Active Ingredient(s): Diclofenac Sodium
Inactive Ingredient(s):
- FERROSOFERRIC OXIDE
- HYPROMELLOSES
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
- CELLULOSE, MICROCRYSTALLINE
- SHELLAC
- POLYETHYLENE GLYCOL 2000
- POVIDONE
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- TALC
- TITANIUM DIOXIDE
Denton Pharma, Inc. Dba Northwind Pharmaceuticals
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
70934-165-30 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
* 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.