Pill Identifier Rabeprazole Sodium - NDC 55700-767
Rabeprazole Sodium
Product Code 55700-767
Rabeprazole Sodium by Quality Care Products, Llc is a yellow rou tablet delayed release about 8 mm in size, imprinted with 20. The product is a human prescription drug with active ingredient(s) rabeprazole sodium.
Rabeprazole Sodium
Active Ingredient(s): Rabeprazole Sodium
Inactive Ingredient(s):
- MANNITOL
- CROSPOVIDONE
- MAGNESIUM OXIDE
- ISOPROPYL ALCOHOL
- SODIUM STEARYL FUMARATE
- MAGNESIUM STEARATE
- ETHYLCELLULOSES
- HYPROMELLOSE PHTHALATE (31% PHTHALATE, 170 CST)
- CARNAUBA WAX
- ALCOHOL
- DIACETYLATED MONOGLYCERIDES
- POLYVINYL ALCOHOL
- TALC
- TITANIUM DIOXIDE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- LECITHIN, SOYBEAN
- FERRIC OXIDE YELLOW
- Shellac
- FERROSOFERRIC OXIDE
- PROPYLENE GLYCOL
- BUTYL ALCOHOL
- AMMONIA
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
Quality Care Products, Llc
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
55700-767-30 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE |
55700-767-60 | 60 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.