Pill Identifier Pantoprazole Sodium - NDC 42291-659
Product Code 42291-659
Pantoprazole Sodium by Avkare, Inc. 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
- ALUMINUM OXIDE
- FD&C YELLOW NO. 6
- HYPROMELLOSE 2910 (15 MPA.S)
- FERROSOFERRIC OXIDE
- FERRIC OXIDE YELLOW
- LACTOSE MONOHYDRATE
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- CELLULOSE, MICROCRYSTALLINE
- POLYETHYLENE GLYCOL 4000
- PROPYLENE GLYCOL
- SHELLAC
- SODIUM CARBONATE
- STEARIC ACID
- TALC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
Avkare, Inc.
Product Type:
Dosage Form:
- Yellow (C48330)
Product Packages
| NDC Package Code | Package Description |
|---|---|
| 42291-659-10 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE |
| 42291-659-50 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE |
| 42291-659-90 | 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.