losartan potassium 25 mg

Generic: losartan potassium

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium 25 mg
Generic Name losartan potassium
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 25 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-675
Product ID 71205-675_e8075254-cdfd-44f3-a9c2-1ed913f846ea
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090382
Listing Expiration 2026-12-31
Marketing Start 2019-10-09

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 71205675
Hyphenated Format 71205-675

Supplemental Identifiers

RxCUI
979485
UPC
0371205675905
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 25 mg (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA090382 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-675-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-675-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-675-90)
source: ndc

Packages (3)

71205-675-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-675-30) 71205-675-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-675-60) 71205-675-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-675-90)

Ingredients (1)

losartan potassium (25 mg/1)

Linked Drug Pages (1)

LOSARTAN POTASSIUM 25 mg ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e8075254-cdfd-44f3-a9c2-1ed913f846ea", "openfda": {"upc": ["0371205675905"], "unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["e8075254-cdfd-44f3-a9c2-1ed913f846ea"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-675-30)", "package_ndc": "71205-675-30", "marketing_start_date": "20220720"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-675-60)", "package_ndc": "71205-675-60", "marketing_start_date": "20220720"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-675-90)", "package_ndc": "71205-675-90", "marketing_start_date": "20220720"}], "brand_name": "LOSARTAN POTASSIUM 25 mg", "product_id": "71205-675_e8075254-cdfd-44f3-a9c2-1ed913f846ea", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71205-675", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "brand_name_suffix": "25 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA090382", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20261231"}