Pill Identifier Pantoprazole Sodium - NDC 67046-534
Product Code 67046-534
Pantoprazole Sodium by Contract Pharmacy Services-pa is a yellow oval about 10 mm in size, imprinted with 93;12. The product is a with active ingredient(s) .
Pantoprazole Sodium
Active Ingredient(s):
Inactive Ingredient(s):
- CALCIUM CARBONATE
- CALCIUM STEARATE
- D&C YELLOW NO. 10
- FD&C YELLOW NO. 6
- HYPROMELLOSE 2910 (15 MPA.S)
- FERROSOFERRIC OXIDE
- FERRIC OXIDE YELLOW
- LACTOSE MONOHYDRATE
- LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE, UNSPECIFIED
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- MICROCRYSTALLINE CELLULOSE
- POLYETHYLENE GLYCOL 4000
- PROPYLENE GLYCOL
- SHELLAC
- SODIUM CARBONATE
- STEARIC ACID
- TALC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
Contract Pharmacy Services-pa
Product Type:
Dosage Form:
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
67046-534-07 | 7 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
67046-534-14 | 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
67046-534-15 | 15 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
67046-534-20 | 20 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
67046-534-21 | 21 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
67046-534-28 | 28 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
67046-534-30 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
67046-534-60 | 60 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
* 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.