Pill Identifier Risedronate Sodium - NDC 16714-870
Risedronate Sodium
Product Code 16714-870
Risedronate Sodium by Northstar Rxllc is a yellow oval tablet delayed release about 12 mm in size, imprinted with s. The product is a human prescription drug with active ingredient(s) risedronate sodium.
Risedronate Sodium
Active Ingredient(s): Risedronate Sodium
Inactive Ingredient(s):
- SILICON DIOXIDE
- EDETATE DISODIUM
- FERRIC OXIDE YELLOW
- HYPROMELLOSE, UNSPECIFIED
- LACTOSE MONOHYDRATE
- MICROCRYSTALLINE CELLULOSE
- POLYSORBATE 80
- SODIUM STEARYL FUMARATE
- TRIETHYL CITRATE
- FERROSOFERRIC OXIDE
- PROPYLENE GLYCOL
- SHELLAC
- TALC
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
Northstar Rxllc
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Yellow (C48330)
Product Packages
NDC Package Code | Package Description |
---|---|
16714-870-02 | 1 DOSE PACK in 1 CARTON > 4 TABLET, DELAYED RELEASE in 1 DOSE PACK (16714-870-01) |
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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.