HUMAN PRESCRIPTION DRUG: 71335-0152

Brand Name: Losartan Potassium and Hydrochlorothiazide

Generic Name: Losartan Potassium and Hydrochlorothiazide

Primary Class: Angiotensin 2 Receptor Antagonists [MoA]

SPL Set ID: 60f3f17d-fd28-406d-97ca-9f01f5f1c72c view on Dailymed | RXCUI: 979468

Manufacturer Name: Bryant Ranch Prepack

Associated Package NDCs
Package NDC Description
71335-0152-1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0152-1)
71335-0152-2 60 TABLET, FILM COATED in 1 BOTTLE (71335-0152-2)
71335-0152-3 30 TABLET, FILM COATED in 1 BOTTLE (71335-0152-3)
71335-0152-4 120 TABLET, FILM COATED in 1 BOTTLE (71335-0152-4)
71335-0152-5 58 TABLET, FILM COATED in 1 BOTTLE (71335-0152-5)
71335-0152-6 100 TABLET, FILM COATED in 1 BOTTLE (71335-0152-6)
71335-0152-7 180 TABLET, FILM COATED in 1 BOTTLE (71335-0152-7)
71335-0152-8 1000 TABLET, FILM COATED in 1 BOTTLE (71335-0152-8)