losartan potassium (71335-1582)

Drug Facts

Product Profile

Brand Name losartan potassium

Generic Name losartan potassium

Labeler bryant ranch prepack

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

losartan potassium 25 mg/1

Manufacturer

Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1582

Product ID 71335-1582_ee7edcfc-8787-49ba-810c-6c4f5d5fa8df

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA203835

Listing Expiration 2026-12-31

Marketing Start 2015-08-19

Pharmacologic Class

Classes

angiotensin 2 receptor antagonists [moa] angiotensin 2 receptor blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351582

Hyphenated Format 71335-1582

Supplemental Identifiers

RxCUI

979480 979485 979492

UNII

3ST302B24A

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 (source: ndc)

Generic Name losartan potassium (source: ndc)

Application Number ANDA203835 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1

source: ndc

Packaging

90 TABLET, FILM COATED in 1 BOTTLE (71335-1582-1)
30 TABLET, FILM COATED in 1 BOTTLE (71335-1582-2)
60 TABLET, FILM COATED in 1 BOTTLE (71335-1582-3)
100 TABLET, FILM COATED in 1 BOTTLE (71335-1582-4)
10 TABLET, FILM COATED in 1 BOTTLE (71335-1582-5)
7 TABLET, FILM COATED in 1 BOTTLE (71335-1582-6)

source: ndc

Packages (6)

71335-1582-1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1582-1) 71335-1582-2 30 TABLET, FILM COATED in 1 BOTTLE (71335-1582-2) 71335-1582-3 60 TABLET, FILM COATED in 1 BOTTLE (71335-1582-3) 71335-1582-4 100 TABLET, FILM COATED in 1 BOTTLE (71335-1582-4) 71335-1582-5 10 TABLET, FILM COATED in 1 BOTTLE (71335-1582-5) 71335-1582-6 7 TABLET, FILM COATED in 1 BOTTLE (71335-1582-6)

Ingredients (1)

losartan potassium (25 mg/1)

Linked Drug Pages (1)

Losartan Potassium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "ee7edcfc-8787-49ba-810c-6c4f5d5fa8df", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["0f3a6984-e601-4a74-9910-49ee5e352d6b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1582-1)", "package_ndc": "71335-1582-1", "marketing_start_date": "20200430"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1582-2)", "package_ndc": "71335-1582-2", "marketing_start_date": "20200430"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1582-3)", "package_ndc": "71335-1582-3", "marketing_start_date": "20200430"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1582-4)", "package_ndc": "71335-1582-4", "marketing_start_date": "20200430"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-1582-5)", "package_ndc": "71335-1582-5", "marketing_start_date": "20200430"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (71335-1582-6)", "package_ndc": "71335-1582-6", "marketing_start_date": "20200430"}], "brand_name": "Losartan Potassium", "product_id": "71335-1582_ee7edcfc-8787-49ba-810c-6c4f5d5fa8df", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-1582", "generic_name": "Losartan Potassium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20261231"}