losartan potassium (65841-731)

Drug Facts

Product Profile

Brand Name losartan potassium

Generic Name losartan potassium

Labeler zydus lifesciences limited

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

losartan potassium 100 mg/1

Manufacturer

Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 65841-731

Product ID 65841-731_36fa833c-716f-4b69-9326-3c54753240dc

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA078243

Listing Expiration 2027-12-31

Marketing Start 2010-10-04

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 65841731

Hyphenated Format 65841-731

Supplemental Identifiers

RxCUI

979480 979485 979492

UNII

3ST302B24A

Packaging Origin

Original Packager

true

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 ANDA078243 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

100 mg/1

source: ndc

Packaging

100 TABLET, FILM COATED in 1 BOTTLE (65841-731-01)
30 TABLET, FILM COATED in 1 BOTTLE (65841-731-06)
1000 TABLET, FILM COATED in 1 BOTTLE (65841-731-10)
90 TABLET, FILM COATED in 1 BOTTLE (65841-731-16)
10 BLISTER PACK in 1 CARTON (65841-731-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65841-731-30)

source: ndc

Packages (5)

65841-731-01 100 TABLET, FILM COATED in 1 BOTTLE (65841-731-01) 65841-731-06 30 TABLET, FILM COATED in 1 BOTTLE (65841-731-06) 65841-731-10 1000 TABLET, FILM COATED in 1 BOTTLE (65841-731-10) 65841-731-16 90 TABLET, FILM COATED in 1 BOTTLE (65841-731-16) 65841-731-77 10 BLISTER PACK in 1 CARTON (65841-731-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65841-731-30)

Ingredients (1)

losartan potassium (100 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": "36fa833c-716f-4b69-9326-3c54753240dc", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["9ccd6823-e813-472c-99cd-c6ef25e74bed"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65841-731-01)", "package_ndc": "65841-731-01", "marketing_start_date": "20101004"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65841-731-06)", "package_ndc": "65841-731-06", "marketing_start_date": "20101004"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65841-731-10)", "package_ndc": "65841-731-10", "marketing_start_date": "20101004"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65841-731-16)", "package_ndc": "65841-731-16", "marketing_start_date": "20101004"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65841-731-77)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (65841-731-30)", "package_ndc": "65841-731-77", "marketing_start_date": "20101004"}], "brand_name": "Losartan Potassium", "product_id": "65841-731_36fa833c-716f-4b69-9326-3c54753240dc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "65841-731", "generic_name": "Losartan Potassium", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA078243", "marketing_category": "ANDA", "marketing_start_date": "20101004", "listing_expiration_date": "20271231"}