losartan potassium tablets, 50 mg
Generic: losartan potassium
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
losartan potassium tablets, 50 mg
Generic Name
losartan potassium
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
losartan potassium 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-1697
Product ID
72162-1697_de41cf4b-8134-42e1-83fb-c63b9041a72b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201170
Listing Expiration
2026-12-31
Marketing Start
2012-09-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721621697
Hyphenated Format
72162-1697
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 tablets, 50 mg (source: ndc)
Generic Name
losartan potassium (source: ndc)
Application Number
ANDA201170 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 1000 TABLET in 1 BOTTLE (72162-1697-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "de41cf4b-8134-42e1-83fb-c63b9041a72b", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["d67926b0-c22b-4803-b55d-c98a81389449"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1697-0)", "package_ndc": "72162-1697-0", "marketing_start_date": "20240206"}], "brand_name": "Losartan potassium Tablets, 50 mg", "product_id": "72162-1697_de41cf4b-8134-42e1-83fb-c63b9041a72b", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72162-1697", "generic_name": "losartan potassium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan potassium Tablets, 50 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA201170", "marketing_category": "ANDA", "marketing_start_date": "20120918", "listing_expiration_date": "20261231"}