Pill Identifier Ropinirole - NDC 0781-5788
Ropinirole
Product Code 0781-5788
Ropinirole by Sandoz Inc is a gree capsule tablet film coated extended release about 13 mm in size, imprinted with sz;162. The product is a human prescription drug with active ingredient(s) ropinirole.
Ropinirole
Active Ingredient(s): Ropinirole
Inactive Ingredient(s):
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
- SILICON DIOXIDE
- HYDROGENATED CASTOR OIL
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
- HYPROMELLOSE, UNSPECIFIED
- ANHYDROUS LACTOSE
- MAGNESIUM STEARATE
- TALC
- POLYETHYLENE GLYCOL, UNSPECIFIED
- FERROSOFERRIC OXIDE
- TITANIUM DIOXIDE
- DIETHYL PHTHALATE
- MALTODEXTRIN
- FERRIC OXIDE YELLOW
- FD&C BLUE NO. 2
- ETHYLCELLULOSE, UNSPECIFIED
Sandoz Inc
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- Green (C48329)
Product Packages
NDC Package Code | Package Description |
---|---|
0781-5788-31 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
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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.