losartan potassium

Generic: losartan

Labeler: granules india ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium
Generic Name losartan
Labeler granules india ltd
Dosage Form TABLET
Routes
ORAL
Active Ingredients

losartan potassium 50 mg/1

Manufacturer
Granules India Ltd

Identifiers & Regulatory

Product NDC 62207-742
Product ID 62207-742_39e0a359-f9d7-c3fb-e063-6394a90a86a8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215959
Listing Expiration 2026-12-31
Marketing Start 2023-03-08

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 62207742
Hyphenated Format 62207-742

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0362207743549 0362207742542 0362207741545
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 (source: ndc)
Application Number ANDA215959 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (62207-742-49)
  • 30 TABLET in 1 BOTTLE (62207-742-54)
source: ndc

Packages (2)

62207-742-49 1000 TABLET in 1 BOTTLE (62207-742-49) 62207-742-54 30 TABLET in 1 BOTTLE (62207-742-54)

Ingredients (1)

losartan potassium (50 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": "39e0a359-f9d7-c3fb-e063-6394a90a86a8", "openfda": {"upc": ["0362207743549", "0362207742542", "0362207741545"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["f9953f51-f30a-952d-e053-6394a90abf5f"], "manufacturer_name": ["Granules India Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (62207-742-49)", "package_ndc": "62207-742-49", "marketing_start_date": "20250318"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62207-742-54)", "package_ndc": "62207-742-54", "marketing_start_date": "20250318"}], "brand_name": "Losartan Potassium", "product_id": "62207-742_39e0a359-f9d7-c3fb-e063-6394a90a86a8", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "62207-742", "generic_name": "Losartan", "labeler_name": "Granules India Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA215959", "marketing_category": "ANDA", "marketing_start_date": "20230308", "listing_expiration_date": "20261231"}