losortan potassium

Generic: losartan potassium

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losortan potassium
Generic Name losartan potassium
Labeler avpak
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 100 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-506
Product ID 50268-506_47e73292-3507-3131-e063-6294a90a0de6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078243
Listing Expiration 2027-12-31
Marketing Start 2020-05-29

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 50268506
Hyphenated Format 50268-506

Supplemental Identifiers

RxCUI
979480 979485 979492
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 losortan potassium (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA078243 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-506-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-506-11)
source: ndc

Packages (1)

50268-506-15 50 BLISTER PACK in 1 BOX (50268-506-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-506-11)

Ingredients (1)

losartan potassium (100 mg/1)

Linked Drug Pages (1)

Losortan Potassium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47e73292-3507-3131-e063-6294a90a0de6", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["a6cd0b5f-2bd6-bed9-e053-2995a90a3191"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-506-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-506-11)", "package_ndc": "50268-506-15", "marketing_start_date": "20200529"}], "brand_name": "Losortan Potassium", "product_id": "50268-506_47e73292-3507-3131-e063-6294a90a0de6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50268-506", "generic_name": "Losartan Potassium", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losortan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA078243", "marketing_category": "ANDA", "marketing_start_date": "20200529", "listing_expiration_date": "20271231"}