losartan potassium
Generic: losartan potassium
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
losartan potassium
Generic Name
losartan potassium
Labeler
american health packaging
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
losartan potassium 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68084-346
Product ID
68084-346_23aa9d46-bb06-0f79-e063-6394a90a21a0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078243
Listing Expiration
2026-12-31
Marketing Start
2010-10-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68084346
Hyphenated Format
68084-346
Supplemental Identifiers
RxCUI
UNII
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
ANDA078243 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-346-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-346-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "23aa9d46-bb06-0f79-e063-6394a90a21a0", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["e7f6b25b-ec4c-4c3a-a541-617d2d9ab393"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-346-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-346-11)", "package_ndc": "68084-346-01", "marketing_start_date": "20101012"}], "brand_name": "Losartan Potassium", "product_id": "68084-346_23aa9d46-bb06-0f79-e063-6394a90a21a0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68084-346", "generic_name": "Losartan Potassium", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA078243", "marketing_category": "ANDA", "marketing_start_date": "20101012", "listing_expiration_date": "20261231"}