losartan potassium 50 mg

Generic: losartan potassium

Labeler: strides pharma science limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium 50 mg
Generic Name losartan potassium
Labeler strides pharma science limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 50 mg/1

Manufacturer
Strides Pharma Science Limited

Identifiers & Regulatory

Product NDC 64380-934
Product ID 64380-934_bf3fbbc7-ee52-466f-b5aa-3c6f8cebed32
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090382
Listing Expiration 2026-12-31
Marketing Start 2019-10-09

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 64380934
Hyphenated Format 64380-934

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0364380933052 0364380935056 0364380935087 0364380935049 0364380934042 0364380933045 0364380934080 0364380933083 0364380934059
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 50 mg (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA090382 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (64380-934-04)
  • 90 TABLET, FILM COATED in 1 BOTTLE (64380-934-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (64380-934-08)
source: ndc

Packages (3)

64380-934-04 30 TABLET, FILM COATED in 1 BOTTLE (64380-934-04) 64380-934-05 90 TABLET, FILM COATED in 1 BOTTLE (64380-934-05) 64380-934-08 1000 TABLET, FILM COATED in 1 BOTTLE (64380-934-08)

Ingredients (1)

losartan potassium (50 mg/1)

Linked Drug Pages (1)

LOSARTAN POTASSIUM 25 mg, LOSARTAN POTASSIUM 50 mg, LOSARTAN POTASSIUM 100 mg ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bf3fbbc7-ee52-466f-b5aa-3c6f8cebed32", "openfda": {"upc": ["0364380933052", "0364380935056", "0364380935087", "0364380935049", "0364380934042", "0364380933045", "0364380934080", "0364380933083", "0364380934059"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["a8817f22-8478-49b9-8354-ab27ca222c6b"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (64380-934-04)", "package_ndc": "64380-934-04", "marketing_start_date": "20191009"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (64380-934-05)", "package_ndc": "64380-934-05", "marketing_start_date": "20191009"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (64380-934-08)", "package_ndc": "64380-934-08", "marketing_start_date": "20191009"}], "brand_name": "LOSARTAN POTASSIUM 50 mg", "product_id": "64380-934_bf3fbbc7-ee52-466f-b5aa-3c6f8cebed32", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "64380-934", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "brand_name_suffix": "50 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA090382", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20261231"}