Pill Identifier Pantoprazole Sodium - NDC 55700-318
Pantoprazole Sodium
Product Code 55700-318
Pantoprazole Sodium by Lake Erie Medical Dba Quality Care Products Llc is a yellow oval tablet delayed release about 11 mm in size, imprinted with m;p9. The product is a human prescription drug with active ingredient(s) pantoprazole sodium.
Pantoprazole Sodium
Active Ingredient(s): Pantoprazole Sodium
Inactive Ingredient(s):
- AMMONIA
- FERROSOFERRIC OXIDE
- CALCIUM STEARATE
- CROSPOVIDONE
- HYPROMELLOSES
- MANNITOL
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- POVIDONE, UNSPECIFIED
- PROPYLENE GLYCOL
- SODIUM CARBONATE
- SHELLAC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
- FERRIC OXIDE YELLOW
Lake Erie Medical Dba Quality Care Products Llc
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
55700-318-60 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
* 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.