losartan potassium

Generic: losartan potassium

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-955
Product ID 43063-955_3fa415e5-6e5f-d2b5-e063-6294a90ad198
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090083
Listing Expiration 2026-12-31
Marketing Start 2010-10-06

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 43063955
Hyphenated Format 43063-955

Supplemental Identifiers

RxCUI
979492
UPC
0343063955901
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 ANDA090083 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-955-90)
source: ndc

Packages (1)

43063-955-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-955-90)

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": "3fa415e5-6e5f-d2b5-e063-6294a90ad198", "openfda": {"upc": ["0343063955901"], "unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["5f7612dc-dccf-49e2-b541-3dab9dc1f97a"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-955-90)", "package_ndc": "43063-955-90", "marketing_start_date": "20190306"}], "brand_name": "Losartan Potassium", "product_id": "43063-955_3fa415e5-6e5f-d2b5-e063-6294a90ad198", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "43063-955", "generic_name": "Losartan Potassium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}