losartan potassium

Generic: losartan potassium

Labeler: legacy pharmaceutical packaging, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler legacy pharmaceutical packaging, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 50 mg/1

Manufacturer
Legacy Pharmaceutical Packaging, LLC

Identifiers & Regulatory

Product NDC 68645-599
Product ID 68645-599_47433131-14e4-7dc8-e063-6394a90a0090
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 68645599
Hyphenated Format 68645-599

Supplemental Identifiers

RxCUI
979492
UPC
0368645599540
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 (68645-599-54)
source: ndc

Packages (1)

68645-599-54 30 TABLET, FILM COATED in 1 BOTTLE (68645-599-54)

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": "47433131-14e4-7dc8-e063-6394a90a0090", "openfda": {"upc": ["0368645599540"], "unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["e5bddb89-37d3-86d0-e053-2a95a90af4f4"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68645-599-54)", "package_ndc": "68645-599-54", "marketing_start_date": "20220808"}], "brand_name": "Losartan Potassium", "product_id": "68645-599_47433131-14e4-7dc8-e063-6394a90a0090", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68645-599", "generic_name": "Losartan potassium", "labeler_name": "Legacy Pharmaceutical Packaging, 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"}