losartan potassium

Generic: losartan potassium

Labeler: macleods pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler macleods pharmaceuticals limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 100 mg/1

Manufacturer
Macleods Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 33342-046
Product ID 33342-046_81824d1f-61f4-457c-8723-cd43d5429029
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202230
Listing Expiration 2026-12-31
Marketing Start 2012-06-01

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 33342046
Hyphenated Format 33342-046

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 potassium (source: ndc)
Application Number ANDA202230 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (33342-046-07)
  • 90 TABLET, FILM COATED in 1 BOTTLE (33342-046-10)
  • 10 BLISTER PACK in 1 CARTON (33342-046-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • 1000 TABLET, FILM COATED in 1 BOTTLE (33342-046-44)
source: ndc

Packages (4)

33342-046-07 30 TABLET, FILM COATED in 1 BOTTLE (33342-046-07) 33342-046-10 90 TABLET, FILM COATED in 1 BOTTLE (33342-046-10) 33342-046-12 10 BLISTER PACK in 1 CARTON (33342-046-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK 33342-046-44 1000 TABLET, FILM COATED in 1 BOTTLE (33342-046-44)

Ingredients (1)

losartan potassium (100 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": "81824d1f-61f4-457c-8723-cd43d5429029", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["85d69d02-c5ef-467e-94aa-903100218795"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (33342-046-07)", "package_ndc": "33342-046-07", "marketing_start_date": "20120601"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (33342-046-10)", "package_ndc": "33342-046-10", "marketing_start_date": "20120601"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-046-12)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "33342-046-12", "marketing_start_date": "20120601"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (33342-046-44)", "package_ndc": "33342-046-44", "marketing_start_date": "20160118"}], "brand_name": "Losartan potassium", "product_id": "33342-046_81824d1f-61f4-457c-8723-cd43d5429029", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "33342-046", "generic_name": "Losartan potassium", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA202230", "marketing_category": "ANDA", "marketing_start_date": "20120601", "listing_expiration_date": "20261231"}