losartan potassium

Generic: losartan

Labeler: granules pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan
Labeler granules pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

losartan potassium 25 mg/1

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-741
Product ID 70010-741_451da3de-077d-522d-e063-6394a90a3537
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215959
Listing Expiration 2026-12-31
Marketing Start 2023-03-08

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 70010741
Hyphenated Format 70010-741

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 (source: ndc)
Application Number ANDA215959 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (70010-741-03)
  • 90 TABLET in 1 BOTTLE (70010-741-09)
  • 1000 TABLET in 1 BOTTLE (70010-741-10)
source: ndc

Packages (3)

70010-741-03 30 TABLET in 1 BOTTLE (70010-741-03) 70010-741-09 90 TABLET in 1 BOTTLE (70010-741-09) 70010-741-10 1000 TABLET in 1 BOTTLE (70010-741-10)

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": "451da3de-077d-522d-e063-6394a90a3537", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["ca012edc-923d-4ada-a261-db82b71b3c4f"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (70010-741-03)", "package_ndc": "70010-741-03", "marketing_start_date": "20230308"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70010-741-09)", "package_ndc": "70010-741-09", "marketing_start_date": "20230308"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70010-741-10)", "package_ndc": "70010-741-10", "marketing_start_date": "20230308"}], "brand_name": "Losartan Potassium", "product_id": "70010-741_451da3de-077d-522d-e063-6394a90a3537", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70010-741", "generic_name": "Losartan", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA215959", "marketing_category": "ANDA", "marketing_start_date": "20230308", "listing_expiration_date": "20261231"}