losortan potassium

Generic: losartan potassium

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

Drug Facts

Product Profile

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

losartan potassium 25 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8639
Product ID 68788-8639_42e81308-557d-4007-b6b6-06b181e923b3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078243
Listing Expiration 2026-12-31
Marketing Start 2024-04-18

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 687888639
Hyphenated Format 68788-8639

Supplemental Identifiers

RxCUI
979485
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 losortan potassium (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA078243 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (68788-8639-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-8639-3)
  • 50 TABLET, FILM COATED in 1 BOTTLE (68788-8639-5)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-8639-6)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-8639-9)
source: ndc

Packages (5)

68788-8639-1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8639-1) 68788-8639-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-8639-3) 68788-8639-5 50 TABLET, FILM COATED in 1 BOTTLE (68788-8639-5) 68788-8639-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-8639-6) 68788-8639-9 90 TABLET, FILM COATED in 1 BOTTLE (68788-8639-9)

Ingredients (1)

losartan potassium (25 mg/1)

Linked Drug Pages (1)

Losortan Potassium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "42e81308-557d-4007-b6b6-06b181e923b3", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["25651749-8950-43ff-bcbd-3bb85f57a360"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-8639-1)", "package_ndc": "68788-8639-1", "marketing_start_date": "20240418"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8639-3)", "package_ndc": "68788-8639-3", "marketing_start_date": "20240418"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (68788-8639-5)", "package_ndc": "68788-8639-5", "marketing_start_date": "20240418"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8639-6)", "package_ndc": "68788-8639-6", "marketing_start_date": "20240418"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8639-9)", "package_ndc": "68788-8639-9", "marketing_start_date": "20240418"}], "brand_name": "Losortan Potassium", "product_id": "68788-8639_42e81308-557d-4007-b6b6-06b181e923b3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68788-8639", "generic_name": "Losartan Potassium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losortan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA078243", "marketing_category": "ANDA", "marketing_start_date": "20240418", "listing_expiration_date": "20261231"}