losartan potassium tablets, 50 mg

Generic: losartan potassium

Labeler: jubilant cadista pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium tablets, 50 mg
Generic Name losartan potassium
Labeler jubilant cadista pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

losartan potassium 50 mg/1

Manufacturer
Jubilant Cadista Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 59746-334
Product ID 59746-334_cfcfa1c5-48d3-4370-aa10-e1d054c1844f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201170
Listing Expiration 2027-12-31
Marketing Start 2012-09-18

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 59746334
Hyphenated Format 59746-334

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0359746333300 0359746335304 0359746334307
UNII
3ST302B24A

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (59746-334-01)
  • 1000 TABLET in 1 BOTTLE (59746-334-10)
  • 30 TABLET in 1 BOTTLE (59746-334-30)
  • 90 TABLET in 1 BOTTLE (59746-334-90)
source: ndc

Packages (4)

59746-334-01 100 TABLET in 1 BOTTLE (59746-334-01) 59746-334-10 1000 TABLET in 1 BOTTLE (59746-334-10) 59746-334-30 30 TABLET in 1 BOTTLE (59746-334-30) 59746-334-90 90 TABLET in 1 BOTTLE (59746-334-90)

Ingredients (1)

losartan potassium (50 mg/1)

Linked Drug Pages (1)

Losartan potassium Tablets, 25 mg, Losartan potassium Tablets, 50 mg, Losartan potassium Tablets, 100 mg ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cfcfa1c5-48d3-4370-aa10-e1d054c1844f", "openfda": {"upc": ["0359746333300", "0359746335304", "0359746334307"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["1bf520a2-a50e-a6ae-0fdf-9be4e69729c0"], "manufacturer_name": ["Jubilant Cadista Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59746-334-01)", "package_ndc": "59746-334-01", "marketing_start_date": "20120918"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59746-334-10)", "package_ndc": "59746-334-10", "marketing_start_date": "20120918"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (59746-334-30)", "package_ndc": "59746-334-30", "marketing_start_date": "20120918"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (59746-334-90)", "package_ndc": "59746-334-90", "marketing_start_date": "20120918"}], "brand_name": "Losartan potassium Tablets, 50 mg", "product_id": "59746-334_cfcfa1c5-48d3-4370-aa10-e1d054c1844f", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "59746-334", "generic_name": "losartan potassium", "labeler_name": "Jubilant Cadista Pharmaceuticals Inc.", "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": "20271231"}