losartan potassium

Generic: losartan potassium

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 50 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-207
Product ID 71610-207_efa818c7-3f30-4f41-9071-71e298ae171d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091497
Listing Expiration 2026-12-31
Marketing Start 2014-07-30

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 71610207
Hyphenated Format 71610-207

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 ANDA091497 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71610-207-30)
  • 45 TABLET, FILM COATED in 1 BOTTLE (71610-207-45)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71610-207-60)
source: ndc

Packages (3)

71610-207-30 30 TABLET, FILM COATED in 1 BOTTLE (71610-207-30) 71610-207-45 45 TABLET, FILM COATED in 1 BOTTLE (71610-207-45) 71610-207-60 90 TABLET, FILM COATED in 1 BOTTLE (71610-207-60)

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": "efa818c7-3f30-4f41-9071-71e298ae171d", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["1f55aaa2-5848-47e0-bba0-6a70b2fa05dd"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-207-30)", "package_ndc": "71610-207-30", "marketing_start_date": "20181214"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71610-207-45)", "package_ndc": "71610-207-45", "marketing_start_date": "20181214"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71610-207-60)", "package_ndc": "71610-207-60", "marketing_start_date": "20181214"}], "brand_name": "Losartan Potassium", "product_id": "71610-207_efa818c7-3f30-4f41-9071-71e298ae171d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71610-207", "generic_name": "Losartan potassium", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA091497", "marketing_category": "ANDA", "marketing_start_date": "20140730", "listing_expiration_date": "20261231"}