Pill Identifier Diclofenac Sodium - NDC 68001-280
Diclofenac Sodium
Product Code 68001-280
Diclofenac Sodium by Bluepoint Laboratories is a brow rou tablet delayed release about 8 mm in size, imprinted with p;50. The product is a human prescription drug with active ingredient(s) diclofenac sodium.
Diclofenac Sodium
Active Ingredient(s): Diclofenac Sodium
Inactive Ingredient(s):
- LACTOSE MONOHYDRATE
- MICROCRYSTALLINE CELLULOSE
- CROSCARMELLOSE SODIUM
- POVIDONE, UNSPECIFIED
- TALC
- MAGNESIUM STEARATE
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- POLYETHYLENE GLYCOL, UNSPECIFIED
- TITANIUM DIOXIDE
- HYPROMELLOSE, UNSPECIFIED
- FERRIC OXIDE RED
- FERRIC OXIDE YELLOW
Bluepoint Laboratories
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Brown (C48332)
Product Packages
NDC Package Code | Package Description |
---|---|
68001-280-00 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE |
68001-280-06 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE |
68001-280-08 | 1000 TABLET, 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.