Pill Identifier Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide - NDC 57664-799
Olmesartan Medoxomil, Amlodipine Besylate And Hydrochlorothiazide
Product Code 57664-799
Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide by Sun Pharmaceutical Industries, Inc. is a re rou tablet film coated about 10 mm in size, imprinted with c55. The product is a human prescription drug with active ingredient(s) olmesartan medoxomil, amlodipine besylate and hydrochlorothiazide.
Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
Active Ingredient(s): Olmesartan Medoxomil, Amlodipine Besylate And Hydrochlorothiazide
View NDC 57664-799Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Red (C48326)
Product Packages
NDC Package Code | Package Description |
---|---|
57664-799-83 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
57664-799-99 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
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Pill Identification data last updated on: December, 2018
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