Pill Identifier Losartan Potassium And Hydrochlorothiazide - NDC 68382-143
Losartan Potassium And Hydrochlorothiazide
Product Code 68382-143
Losartan Potassium And Hydrochlorothiazide by Zydus Pharmaceuticals (usa) Inc. is a white capsule tablet film coated about 13 mm in size, imprinted with zd19. The product is a human prescription drug with active ingredient(s) losartan potassium and hydrochlorothiazide.
Losartan Potassium And Hydrochlorothiazide
Active Ingredient(s): Losartan Potassium And Hydrochlorothiazide
Inactive Ingredient(s):
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED
- HYPROMELLOSES
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- STARCH, CORN
- CELLULOSE, MICROCRYSTALLINE
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- TALC
- TITANIUM DIOXIDE
- SILICON DIOXIDE
- POLYETHYLENE GLYCOL, UNSPECIFIED
Image of Losartan Potassium And Hydrochlorothiazide tablet, film coated by Zydus Pharmaceuticals (usa) Inc.
Zydus Pharmaceuticals (usa) Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
68382-143-06 | 30 TABLET, FILM COATED in 1 BOTTLE |
68382-143-10 | 1000 TABLET, FILM COATED in 1 BOTTLE |
68382-143-16 | 90 TABLET, FILM COATED in 1 BOTTLE |
68382-143-23 | 4000 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.