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 25 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-029
Product ID 72789-029_2d58db43-e7d1-439f-e063-6294a90a6043
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203835
Listing Expiration 2026-12-31
Marketing Start 2015-08-19

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 72789029
Hyphenated Format 72789-029

Supplemental Identifiers

RxCUI
979485
UPC
0372789029306
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 ANDA203835 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-14)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-90)
source: ndc

Packages (3)

72789-029-14 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-14) 72789-029-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-30) 72789-029-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-90)

Ingredients (1)

losartan potassium (25 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": "2d58db43-e7d1-439f-e063-6294a90a6043", "openfda": {"upc": ["0372789029306"], "unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["1843ee4b-1afc-4992-993a-4b0e03e785fc"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-14)", "package_ndc": "72789-029-14", "marketing_start_date": "20200924"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-30)", "package_ndc": "72789-029-30", "marketing_start_date": "20231206"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-029-90)", "package_ndc": "72789-029-90", "marketing_start_date": "20191120"}], "brand_name": "Losartan Potassium", "product_id": "72789-029_2d58db43-e7d1-439f-e063-6294a90a6043", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72789-029", "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": "25 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20261231"}