Pill Identifier Ropinirole - NDC 55111-662
Ropinirole
Product Code 55111-662
Ropinirole by Dr. Reddys Laboratories Limited is a re capsule tablet film coated extended release about 12 mm in size, imprinted with r8. The product is a human prescription drug with active ingredient(s) ropinirole.
Ropinirole
Active Ingredient(s): Ropinirole
Inactive Ingredient(s):
- anhydrous lactose
- carboxymethylcellulose sodium
- silicon dioxide
- Hypromellose, Unspecified
- magnesium stearate
- POLYETHYLENE GLYCOL, UNSPECIFIED
- povidone
- TITANIUM DIOXIDE
- triethyl citrate
- FERRIC OXIDE YELLOW
- FERROSOFERRIC OXIDE
- ETHYLCELLULOSES
- FERRIC OXIDE RED
Dr. Reddys Laboratories Limited
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- Red (C48326)
Product Packages
NDC Package Code | Package Description |
---|---|
55111-662-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
55111-662-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
55111-662-90 | 90 TABLET, FILM COATED, EXTENDED 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.