Pill Identifier Oxybutynin Chloride Extended Release - NDC 35356-991
Product Code 35356-991
Oxybutynin Chloride Extended Release by Lake Erie Medical Dba Quality Care Products Llc is a white rou about 7 mm in size, imprinted with ku;270. The product is a with active ingredient(s) .
Oxybutynin Chloride Extended Release
Active Ingredient(s):
Inactive Ingredient(s):
- ANHYDROUS LACTOSE
- LACTOSE MONOHYDRATE
- MANNITOL
- ANHYDROUS DEXTROSE
- TARTARIC ACID
- SILICON DIOXIDE
- MAGNESIUM STEARATE
- CELLULOSE ACETATE
- POLYETHYLENE GLYCOL 400
- TITANIUM DIOXIDE
- FERROSOFERRIC OXIDE
- PROPYLENE GLYCOL
- HYPROMELLOSE 2208 (100 MPA.S)
- TRIACETIN
Lake Erie Medical Dba Quality Care Products Llc
Product Type:
Dosage Form:
- White (C48325)
Product Packages
| NDC Package Code | Package Description |
|---|---|
| 35356-991-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE |
| 35356-991-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE |
| 35356-991-90 | 90 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.