Pill Identifier Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide - NDC 49884-788
Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide
Product Code 49884-788
Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide by Endo Usa, Inc. is a white oval tablet film coated about 15 mm in size, imprinted with p;788. The product is a human prescription drug with active ingredient(s) olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide.
Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide
Active Ingredient(s): Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide
Inactive Ingredient(s):
- CELLULOSE, MICROCRYSTALLINE
- STARCH, CORN
- CROSCARMELLOSE SODIUM
- MAGNESIUM STEARATE
- TITANIUM DIOXIDE
- HYPROMELLOSE 2208 (100 MPA.S)
- POLYETHYLENE GLYCOL 1000
- POLYSORBATE 20
- POLYVINYL ALCOHOL (100000 MW)
Endo Usa, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- White (C48325)
Product Packages
| NDC Package Code | Package Description |
|---|---|
| 49884-788-09 | 90 TABLET, FILM COATED in 1 BOTTLE |
| 49884-788-11 | 30 TABLET, FILM COATED 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.