Pill Identifier Oxybutynin Chloride Extended Release - NDC 71335-0669
Oxybutynin Chloride
Product Code 71335-0669
Oxybutynin Chloride Extended Release by Bryant Ranch Prepack is a white rou tablet extended release about 8 mm in size, imprinted with ku;271. The product is a human prescription drug with active ingredient(s) oxybutynin chloride.
Oxybutynin Chloride Extended Release
Active Ingredient(s): Oxybutynin Chloride
Inactive Ingredient(s):
- FERROSOFERRIC OXIDE
- CELLULOSE ACETATE
- SILICON DIOXIDE
- ANHYDROUS DEXTROSE
- HYPROMELLOSE, UNSPECIFIED
- ANHYDROUS LACTOSE
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- MANNITOL
- POLYETHYLENE GLYCOL 400
- PROPYLENE GLYCOL
- TARTARIC ACID
- TITANIUM DIOXIDE
- TRIACETIN
Bryant Ranch Prepack
Product Type: Human Prescription Drug
Dosage Form: Tablet, Extended Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
71335-0669-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE |
71335-0669-2 | 18 TABLET, EXTENDED RELEASE in 1 BOTTLE |
71335-0669-3 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE |
71335-0669-4 | 60 TABLET, EXTENDED 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.