diclofenac sodium and misoprostol
diclofenac sodium and misoprostol is listed in the FDA National Drug Code directory with 7 NDC codes, marketed under brand names including Diclofenac Sodium Misoprostol, ARTHROTEC. Available dosage forms: tablet, delayed release, tablet, film coated.
Drug Details
- Generic Name
- diclofenac sodium and misoprostol
- Brand Names
- Diclofenac Sodium Misoprostol, ARTHROTEC
- Application Number
- ANDA205143
- Sponsor
- Bryant Ranch Prepack
- NDC Codes
- 7
- Dosage Forms
- TABLET, DELAYED RELEASE, TABLET, FILM COATED
- Routes
- ORAL
- Active Ingredients
- DICLOFENAC SODIUM, MISOPROSTOL
Indications and Usage
1 INDICATIONS AND USAGE Diclofenac sodium and misoprostol delayed-release tablets are indicated for treatment of the signs and symptoms of osteoarthritis or rheumatoid arthritis in adult patients at high risk of developing NSAID-induced gastric and duodenal ulcers and their complications. For a list of factors that may increase the risk of NSAID-induced gastric and duodenal ulcers and their complications [see Warnings and Precautions (5.3) ] . Diclofenac sodium and misoprostol delayed-release tablets are a combination of diclofenac sodium, a non-steroidal anti-inflammatory drug, and misoprostol, a prostaglandin-1 (PGE1) analog, indicated for the treatment of signs and symptoms of osteoarthritis or rheumatoid arthritis in adult patients at high risk of developing NSAID-induced gastric and duodenal ulcers and their complications. ( 1 )