losartan potassium

Generic: losartan potassium

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

Drug Facts

Product Profile

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

losartan potassium 100 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-029
Product ID 62332-029_a12a7eb0-196c-4ddc-ba64-2909f65b6f19
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090428
Listing Expiration 2026-12-31
Marketing Start 2016-05-23

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 62332029
Hyphenated Format 62332-029

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0362332028306 0362332027309 0362332029303
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 ANDA090428 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (62332-029-30)
  • 100 TABLET, FILM COATED in 1 BOTTLE (62332-029-31)
  • 90 TABLET, FILM COATED in 1 BOTTLE (62332-029-90)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (62332-029-91)
source: ndc

Packages (4)

62332-029-30 30 TABLET, FILM COATED in 1 BOTTLE (62332-029-30) 62332-029-31 100 TABLET, FILM COATED in 1 BOTTLE (62332-029-31) 62332-029-90 90 TABLET, FILM COATED in 1 BOTTLE (62332-029-90) 62332-029-91 1000 TABLET, FILM COATED in 1 BOTTLE (62332-029-91)

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": "a12a7eb0-196c-4ddc-ba64-2909f65b6f19", "openfda": {"upc": ["0362332028306", "0362332027309", "0362332029303"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["1dadbe02-289c-4312-9e65-40f3314dcc31"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-029-30)", "package_ndc": "62332-029-30", "marketing_start_date": "20160523"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62332-029-31)", "package_ndc": "62332-029-31", "marketing_start_date": "20160523"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62332-029-90)", "package_ndc": "62332-029-90", "marketing_start_date": "20160523"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-029-91)", "package_ndc": "62332-029-91", "marketing_start_date": "20160523"}], "brand_name": "Losartan Potassium", "product_id": "62332-029_a12a7eb0-196c-4ddc-ba64-2909f65b6f19", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "62332-029", "generic_name": "Losartan Potassium", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA090428", "marketing_category": "ANDA", "marketing_start_date": "20160523", "listing_expiration_date": "20261231"}