losartan potassium

Generic: losartan potassium

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

Drug Facts

Product Profile

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

losartan potassium 50 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7665
Product ID 68788-7665_247e9033-04e4-403d-98bd-acbe40d8f987
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203835
Listing Expiration 2026-12-31
Marketing Start 2020-02-28

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 687887665
Hyphenated Format 68788-7665

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 (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA203835 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (68788-7665-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-7665-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-7665-6)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-7665-9)
source: ndc

Packages (4)

68788-7665-1 100 TABLET, FILM COATED in 1 BOTTLE (68788-7665-1) 68788-7665-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-7665-3) 68788-7665-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-7665-6) 68788-7665-9 90 TABLET, FILM COATED in 1 BOTTLE (68788-7665-9)

Ingredients (1)

losartan potassium (50 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": "247e9033-04e4-403d-98bd-acbe40d8f987", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["fe1df76d-4925-444d-8e30-9dd07f205fb7"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-7665-1)", "package_ndc": "68788-7665-1", "marketing_start_date": "20200228"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7665-3)", "package_ndc": "68788-7665-3", "marketing_start_date": "20200228"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7665-6)", "package_ndc": "68788-7665-6", "marketing_start_date": "20200228"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7665-9)", "package_ndc": "68788-7665-9", "marketing_start_date": "20200228"}], "brand_name": "Losartan Potassium", "product_id": "68788-7665_247e9033-04e4-403d-98bd-acbe40d8f987", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68788-7665", "generic_name": "Losartan Potassium", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20200228", "listing_expiration_date": "20261231"}