losartan potassium 100 mg

Generic: losartan potassium

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

Drug Facts

Product Profile

Brand Name losartan potassium 100 mg
Generic Name losartan potassium
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

losartan potassium 100 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2203
Product ID 68071-2203_1d75df72-5359-f395-e063-6394a90a2fb3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090382
Listing Expiration 2026-12-31
Marketing Start 2019-10-09

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 680712203
Hyphenated Format 68071-2203

Supplemental Identifiers

RxCUI
979480
UPC
0368071220391
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 100 mg (source: ndc)
Generic Name losartan potassium (source: ndc)
Application Number ANDA090382 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (68071-2203-9)
source: ndc

Packages (1)

68071-2203-9 90 TABLET, FILM COATED in 1 BOTTLE (68071-2203-9)

Ingredients (1)

losartan potassium (100 mg/1)

Linked Drug Pages (1)

LOSARTAN POTASSIUM 100 mg ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d75df72-5359-f395-e063-6394a90a2fb3", "openfda": {"upc": ["0368071220391"], "unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["a955160f-3c2d-3366-e053-2a95a90a65ea"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-2203-9)", "package_ndc": "68071-2203-9", "marketing_start_date": "20200630"}], "brand_name": "LOSARTAN POTASSIUM 100 mg", "product_id": "68071-2203_1d75df72-5359-f395-e063-6394a90a2fb3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68071-2203", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "brand_name_suffix": "100 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA090382", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20261231"}