NDC 65862-779 – Olmesartan Medoxomil and Hydrochlorothiazide

Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC65862-779

Product details

Brand name
Olmesartan Medoxomil and Hydrochlorothiazide
Generic name
Olmesartan Medoxomil and Hydrochlorothiazide
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205391
Marketed since
April 24, 2017
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Olmesartan Medoxomil And Hydrochlorothiazide →

Package NDC codes (4)

Package NDCDescriptionSince
65862-779-3030 TABLET, FILM COATED in 1 BOTTLE (65862-779-30)Apr 24, 2017
65862-779-7810 BLISTER PACK in 1 CARTON (65862-779-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-779-10)Apr 24, 2017
65862-779-9090 TABLET, FILM COATED in 1 BOTTLE (65862-779-90)Apr 24, 2017
65862-779-991000 TABLET, FILM COATED in 1 BOTTLE (65862-779-99)Apr 24, 2017

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