Pill Identifier Etodolac - NDC 0093-1122
Etodolac
Product Code 0093-1122
Etodolac by Teva Pharmaceuticals Usa, Inc. is a orange oval tablet film coated extended release about 17 mm in size, imprinted with 93;1122. The product is a human prescription drug with active ingredient(s) etodolac.
Etodolac
Active Ingredient(s): Etodolac
Inactive Ingredient(s):
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE
- CARBOMER 934
- SILICON DIOXIDE
- HYDROXYPROPYL CELLULOSE (90000 WAMW)
- HYPROMELLOSE 2208 (15000 MPA.S)
- HYPROMELLOSE 2910 (5 MPA.S)
- HYPROMELLOSE 2910 (15 MPA.S)
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- POLYETHYLENE GLYCOL 4000
- SODIUM LAURYL SULFATE
- TITANIUM DIOXIDE
- D&C YELLOW NO. 10
- ALUMINUM OXIDE
- FD&C RED NO. 40
- FD&C YELLOW NO. 6
Teva Pharmaceuticals Usa, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- Orange (C48331)
Product Packages
NDC Package Code | Package Description |
---|---|
0093-1122-01 | 100 TABLET, FILM COATED, 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.