losartan potassium

Generic: losartan potassium

Labeler: hisun pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler hisun pharmaceuticals usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 25 mg/1

Manufacturer
Hisun Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 42658-102
Product ID 42658-102_32efe915-7ba2-fb36-e063-6394a90a72ce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204795
Listing Expiration 2026-12-31
Marketing Start 2025-01-01

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 42658102
Hyphenated Format 42658-102

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0358623200315
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 ANDA204795 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42658-102-04)
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42658-102-08)
source: ndc

Packages (2)

42658-102-04 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42658-102-04) 42658-102-08 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42658-102-08)

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": "32efe915-7ba2-fb36-e063-6394a90a72ce", "openfda": {"upc": ["0358623200315"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["9af29d03-7192-4585-8e5f-82474c190af7"], "manufacturer_name": ["Hisun Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42658-102-04)", "package_ndc": "42658-102-04", "marketing_start_date": "20250101"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42658-102-08)", "package_ndc": "42658-102-08", "marketing_start_date": "20250101"}], "brand_name": "LOSARTAN POTASSIUM", "product_id": "42658-102_32efe915-7ba2-fb36-e063-6394a90a72ce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "42658-102", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "Hisun Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA204795", "marketing_category": "ANDA", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}