losartan potassium tablets, 50 mg

Generic: losartan potassium

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium tablets, 50 mg
Generic Name losartan potassium
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

losartan potassium 50 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1817
Product ID 71335-1817_fb077532-f94e-44e1-afd3-6be55c4062c8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201170
Listing Expiration 2026-12-31
Marketing Start 2012-09-18

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 713351817
Hyphenated Format 71335-1817

Supplemental Identifiers

RxCUI
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 tablets, 50 mg (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA201170 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1817-1)
  • 90 TABLET in 1 BOTTLE (71335-1817-2)
  • 60 TABLET in 1 BOTTLE (71335-1817-3)
  • 120 TABLET in 1 BOTTLE (71335-1817-4)
  • 100 TABLET in 1 BOTTLE (71335-1817-5)
  • 180 TABLET in 1 BOTTLE (71335-1817-6)
  • 10 TABLET in 1 BOTTLE (71335-1817-7)
  • 7 TABLET in 1 BOTTLE (71335-1817-8)
source: ndc

Packages (8)

Ingredients (1)

losartan potassium (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fb077532-f94e-44e1-afd3-6be55c4062c8", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["3d7ddcac-508d-459c-96c8-c62f9c0b5193"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1817-1)", "package_ndc": "71335-1817-1", "marketing_start_date": "20211221"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1817-2)", "package_ndc": "71335-1817-2", "marketing_start_date": "20211221"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1817-3)", "package_ndc": "71335-1817-3", "marketing_start_date": "20211221"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1817-4)", "package_ndc": "71335-1817-4", "marketing_start_date": "20211221"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1817-5)", "package_ndc": "71335-1817-5", "marketing_start_date": "20211221"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-1817-6)", "package_ndc": "71335-1817-6", "marketing_start_date": "20211221"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-1817-7)", "package_ndc": "71335-1817-7", "marketing_start_date": "20211221"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE (71335-1817-8)", "package_ndc": "71335-1817-8", "marketing_start_date": "20211221"}], "brand_name": "Losartan potassium Tablets, 50 mg", "product_id": "71335-1817_fb077532-f94e-44e1-afd3-6be55c4062c8", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-1817", "generic_name": "losartan potassium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan potassium Tablets, 50 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA201170", "marketing_category": "ANDA", "marketing_start_date": "20120918", "listing_expiration_date": "20261231"}