Pill Identifier Pantoprazole Sodium - NDC 65162-637
Pantoprazole
Product Code 65162-637
Pantoprazole Sodium by Amneal Pharmaceuticals Llc is a yellow oval tablet delayed release about 11 mm in size, imprinted with a37. The product is a human prescription drug with active ingredient(s) pantoprazole.
Pantoprazole Sodium
Active Ingredient(s): Pantoprazole
Inactive Ingredient(s):
- AMMONIA
- CROSPOVIDONE (12 MPA.S AT 5%)
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED
- HYPROMELLOSES
- FERROSOFERRIC OXIDE
- FERRIC OXIDE YELLOW
- MANNITOL
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POVIDONE
- PROPYLENE GLYCOL
- POLYVINYL ALCOHOL, UNSPECIFIED
- SHELLAC
- SODIUM CARBONATE
- SODIUM HYDROXIDE
- SODIUM STEARYL FUMARATE
- TALC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
Amneal Pharmaceuticals Llc
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
65162-637-03 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE |
65162-637-09 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE |
65162-637-11 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE |
65162-637-50 | 500 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.