losartan potassium

Generic: losartan potassium

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan potassium
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

losartan potassium 100 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-146
Product ID 29300-146_cedb47f7-7b7e-464f-b1ed-2a3afdb074d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203030
Listing Expiration 2026-12-31
Marketing Start 2015-10-14

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 29300146
Hyphenated Format 29300-146

Supplemental Identifiers

RxCUI
979480 979485 979492
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 ANDA203030 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (29300-146-01)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (29300-146-10)
  • 30 TABLET in 1 BOTTLE, PLASTIC (29300-146-13)
  • 90 TABLET in 1 BOTTLE, PLASTIC (29300-146-19)
source: ndc

Packages (4)

29300-146-01 100 TABLET in 1 BOTTLE, PLASTIC (29300-146-01) 29300-146-10 1000 TABLET in 1 BOTTLE, PLASTIC (29300-146-10) 29300-146-13 30 TABLET in 1 BOTTLE, PLASTIC (29300-146-13) 29300-146-19 90 TABLET in 1 BOTTLE, PLASTIC (29300-146-19)

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": "cedb47f7-7b7e-464f-b1ed-2a3afdb074d4", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["92691768-b5e6-4527-98dc-d86c58f6f13e"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (29300-146-01)", "package_ndc": "29300-146-01", "marketing_start_date": "20180228"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (29300-146-10)", "package_ndc": "29300-146-10", "marketing_start_date": "20180228"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (29300-146-13)", "package_ndc": "29300-146-13", "marketing_start_date": "20180228"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (29300-146-19)", "package_ndc": "29300-146-19", "marketing_start_date": "20180228"}], "brand_name": "Losartan Potassium", "product_id": "29300-146_cedb47f7-7b7e-464f-b1ed-2a3afdb074d4", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "29300-146", "generic_name": "Losartan Potassium", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA203030", "marketing_category": "ANDA", "marketing_start_date": "20151014", "listing_expiration_date": "20261231"}