losartan potassium

Generic: losartan potassium

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler remedyrepack inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 25 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3894
Product ID 70518-3894_471733cb-e09a-1fe8-e063-6394a90a09fe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203835
Listing Expiration 2026-12-31
Marketing Start 2023-10-16

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 705183894
Hyphenated Format 70518-3894

Supplemental Identifiers

RxCUI
979485
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
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-0)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-1)
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3894-2)
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-3)
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3894-4)
source: ndc

Packages (5)

70518-3894-0 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-0) 70518-3894-1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-1) 70518-3894-2 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3894-2) 70518-3894-3 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-3) 70518-3894-4 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3894-4)

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": "471733cb-e09a-1fe8-e063-6394a90a09fe", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["45c01cc9-c7d1-4bb6-a105-354fc936ec63"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-0)", "package_ndc": "70518-3894-0", "marketing_start_date": "20231016"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-1)", "package_ndc": "70518-3894-1", "marketing_start_date": "20240725"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3894-2)", "package_ndc": "70518-3894-2", "marketing_start_date": "20250213"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3894-3)", "package_ndc": "70518-3894-3", "marketing_start_date": "20250327"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3894-4)", "package_ndc": "70518-3894-4", "marketing_start_date": "20250726"}], "brand_name": "Losartan Potassium", "product_id": "70518-3894_471733cb-e09a-1fe8-e063-6394a90a09fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "70518-3894", "generic_name": "Losartan Potassium", "labeler_name": "REMEDYREPACK 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": "20231016", "listing_expiration_date": "20261231"}