Pill Identifier Rabeprazole Sodium - NDC 65162-724
Rabeprazole
Product Code 65162-724
Rabeprazole Sodium by Amneal Pharmaceuticals Llc is a yellow rou tablet delayed release about 7 mm in size, imprinted with ar. The product is a human prescription drug with active ingredient(s) rabeprazole.
Rabeprazole Sodium
Active Ingredient(s): Rabeprazole
Inactive Ingredient(s):
- AMMONIA
- CROSPOVIDONE (12 MPA.S AT 5%)
- DIETHYL PHTHALATE
- ETHYLCELLULOSES
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED
- HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST)
- MAGNESIUM OXIDE
- MANNITOL
- MAGNESIUM STEARATE
- PROPYLENE GLYCOL
- FERROSOFERRIC OXIDE
- FERRIC OXIDE YELLOW
- SODIUM STEARYL FUMARATE
- SHELLAC
- TALC
- TITANIUM DIOXIDE
Amneal Pharmaceuticals Llc
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
65162-724-03 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE |
65162-724-09 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE |
65162-724-11 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE |
65162-724-50 | 500 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.