arbli

Generic: losartan potassium

Labeler: scienture llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name arbli
Generic Name losartan potassium
Labeler scienture llc
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

losartan potassium 10 mg/mL

Manufacturer
Scienture LLC

Identifiers & Regulatory

Product NDC 83245-053
Product ID 83245-053_0d6183d3-e8e3-416e-a359-9348c61ac736
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA218772
Listing Expiration 2026-12-31
Marketing Start 2025-03-19

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 83245053
Hyphenated Format 83245-053

Supplemental Identifiers

RxCUI
2709039 2709046
UPC
0383245053063
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 arbli (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number NDA218772 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (83245-053-06) / 165 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

losartan potassium (10 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0d6183d3-e8e3-416e-a359-9348c61ac736", "openfda": {"upc": ["0383245053063"], "unii": ["3ST302B24A"], "rxcui": ["2709039", "2709046"], "spl_set_id": ["afd2d1ba-e7af-4e4e-8b7e-a9f72612fc97"], "manufacturer_name": ["Scienture LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (83245-053-06)  / 165 mL in 1 BOTTLE", "package_ndc": "83245-053-06", "marketing_start_date": "20250319"}], "brand_name": "ARBLI", "product_id": "83245-053_0d6183d3-e8e3-416e-a359-9348c61ac736", "dosage_form": "SUSPENSION", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "83245-053", "generic_name": "losartan potassium", "labeler_name": "Scienture LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ARBLI", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "10 mg/mL"}], "application_number": "NDA218772", "marketing_category": "NDA", "marketing_start_date": "20250319", "listing_expiration_date": "20261231"}