Pill Identifier Pantoprazole Sodium - NDC 50742-151
Pantoprazole Sodium
Product Code 50742-151
Pantoprazole Sodium by Ingenus Pharmaceuticals, Llc is a yellow oval tablet delayed release about 10 mm in size, imprinted with ing151. The product is a human prescription drug with active ingredient(s) pantoprazole sodium.
Pantoprazole Sodium
Active Ingredient(s): Pantoprazole Sodium
Inactive Ingredient(s):
- CROSPOVIDONE
- HYPROMELLOSE 2910 (3 MPA.S)
- CELLULOSE, MICROCRYSTALLINE
- POVIDONE K25
- LACTOSE MONOHYDRATE
- CALCIUM STEARATE
- TALC
- PROPYLENE GLYCOL
- TITANIUM DIOXIDE
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- TRIETHYL CITRATE
- HYPROMELLOSE 2910 (6 MPA.S)
- FERRIC OXIDE YELLOW
- FERROSOFERRIC OXIDE
Ingenus Pharmaceuticals, Llc
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
50742-151-10 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE |
50742-151-90 | 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.