Pill Identifier Pantoprazole Sodium - NDC 72189-112
Pantoprazole
Product Code 72189-112
Pantoprazole Sodium by Direct Rx is a yellow oval tablet delayed release about 9 mm in size, imprinted with h;125. The product is a human prescription drug with active ingredient(s) pantoprazole.
Pantoprazole Sodium
Active Ingredient(s): Pantoprazole
Inactive Ingredient(s):
- PROPYLENE GLYCOL
- LACTOSE MONOHYDRATE
- SODIUM CARBONATE
- AMMONIA
- TRIETHYL CITRATE
- FERROSOFERRIC OXIDE
- HYPROMELLOSES
- POLYSORBATE 80
- SODIUM LAURYL SULFATE
- SHELLAC
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED
- CALCIUM STEARATE
- FERRIC OXIDE YELLOW
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
- TITANIUM DIOXIDE
Direct Rx
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
72189-112-30 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE |
72189-112-60 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE |
72189-112-90 | 90 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.