Pill Identifier Pantoprazole Sodium - NDC 61919-134
Pantoprazole Sodium
Product Code 61919-134
Pantoprazole Sodium by Direct Rx is a yellow oval tablet delayed release about 8 mm in size, imprinted with 93;11. The product is a human prescription drug with active ingredient(s) pantoprazole sodium.
Pantoprazole Sodium
Active Ingredient(s): Pantoprazole Sodium
Inactive Ingredient(s):
- HYPROMELLOSE 2910 (15 MPA.S)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- CELLULOSE, MICROCRYSTALLINE
- PROPYLENE GLYCOL
- STEARIC ACID
- TRIETHYL CITRATE
- CALCIUM STEARATE
- D&C YELLOW NO. 10
- FD&C YELLOW NO. 6
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED
- POLYETHYLENE GLYCOL 4000
- SHELLAC
- SODIUM CARBONATE
- TALC
- TITANIUM DIOXIDE
- LACTOSE MONOHYDRATE
- CALCIUM CARBONATE
- FERROSOFERRIC OXIDE
- FERRIC OXIDE YELLOW
Direct Rx
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
61919-134-90 | 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.