losartan potassium

Generic: losartan potassium

Labeler: lupin pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler lupin pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

losartan potassium 100 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-378
Product ID 68180-378_38431fb6-7157-4be5-929a-0c65b7a29c55
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078232
Listing Expiration 2027-12-31
Marketing Start 2017-11-01

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 68180378
Hyphenated Format 68180-378

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0368180212065 0368180376033 0368180210061 0368180378037 0368180308027 0368180376095 0368180211068 0368180309024 0368180377030
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 losartan potassium (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA078232 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (68180-378-03)
  • 90 TABLET in 1 BOTTLE (68180-378-09)
source: ndc

Packages (2)

68180-378-03 1000 TABLET in 1 BOTTLE (68180-378-03) 68180-378-09 90 TABLET in 1 BOTTLE (68180-378-09)

Ingredients (1)

losartan potassium (100 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": "38431fb6-7157-4be5-929a-0c65b7a29c55", "openfda": {"upc": ["0368180212065", "0368180376033", "0368180210061", "0368180378037", "0368180308027", "0368180376095", "0368180211068", "0368180309024", "0368180377030"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["e5886220-43b7-46e1-9034-5242ba245bd1"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (68180-378-03)", "package_ndc": "68180-378-03", "marketing_start_date": "20171101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68180-378-09)", "package_ndc": "68180-378-09", "marketing_start_date": "20171101"}], "brand_name": "Losartan Potassium", "product_id": "68180-378_38431fb6-7157-4be5-929a-0c65b7a29c55", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68180-378", "generic_name": "Losartan Potassium", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA078232", "marketing_category": "ANDA", "marketing_start_date": "20171101", "listing_expiration_date": "20271231"}