Pill Identifier Pantoprazole Sodium - NDC 71335-0551
Pantoprazole
Product Code 71335-0551
Pantoprazole Sodium by Bryant Ranch Prepack is a yellow oval tablet delayed release about 12 mm in size, imprinted with h;126. The product is a human prescription drug with active ingredient(s) pantoprazole.
Pantoprazole Sodium
Active Ingredient(s): Pantoprazole
Inactive Ingredient(s):
- CALCIUM STEARATE
- FERRIC OXIDE YELLOW
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
- HYPROMELLOSE, UNSPECIFIED
- LACTOSE MONOHYDRATE
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
- POLYSORBATE 80
- PROPYLENE GLYCOL
- SODIUM CARBONATE
- SODIUM LAURYL SULFATE
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
- AMMONIA
- FERROSOFERRIC OXIDE
- SHELLAC
Bryant Ranch Prepack
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
71335-0551-1 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE |
71335-0551-2 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE |
71335-0551-3 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE |
71335-0551-4 | 58 TABLET, DELAYED RELEASE in 1 BOTTLE |
71335-0551-5 | 14 TABLET, DELAYED RELEASE in 1 BOTTLE |
71335-0551-6 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE |
71335-0551-7 | 10 TABLET, DELAYED RELEASE in 1 BOTTLE |
71335-0551-8 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE |
71335-0551-9 | 180 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.