Losartan Potassium and Hydrochlorothiazide (50090-2632)

Drug Facts

Product Profile

Brand Name Losartan Potassium and Hydrochlorothiazide

Generic Name Losartan Potassium and Hydrochlorothiazide

Labeler A-S Medication Solutions

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

HYDROCHLOROTHIAZIDE 12.5 mg/1, LOSARTAN POTASSIUM 50 mg/1

Identifiers & Regulatory

Product NDC 50090-2632

Product ID 50090-2632_d161fe1a-b4d4-48b5-a52f-95c2f8d2f09e

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA091629

Listing Expiration 2026-12-31

Marketing Start 2010-10-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902632

Hyphenated Format 50090-2632

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name Losartan Potassium and Hydrochlorothiazide (source: ndc)

Generic Name Losartan Potassium and Hydrochlorothiazide (source: ndc)

Application Number ANDA091629 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

12.5 mg/1
50 mg/1

source: ndc

Packaging

90 TABLET, FILM COATED in 1 BOTTLE (50090-2632-0)
30 TABLET, FILM COATED in 1 BOTTLE (50090-2632-1)
100 TABLET, FILM COATED in 1 BOTTLE (50090-2632-2)

source: ndc

Packages (3)

50090-2632-0 90 TABLET, FILM COATED in 1 BOTTLE (50090-2632-0) 50090-2632-1 30 TABLET, FILM COATED in 1 BOTTLE (50090-2632-1) 50090-2632-2 100 TABLET, FILM COATED in 1 BOTTLE (50090-2632-2)

Ingredients (2)

HYDROCHLOROTHIAZIDE (12.5 mg/1) LOSARTAN POTASSIUM (50 mg/1)

Linked Drug Pages (1)

Losartan Potassium and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

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