losartan potassium

Generic: losartan potassium

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

Drug Facts

Product Profile

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

losartan potassium 100 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-702
Product ID 31722-702_40b34aeb-20b5-4200-e063-6394a90a96e9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203835
Listing Expiration 2026-12-31
Marketing Start 2015-08-19

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 31722702
Hyphenated Format 31722-702

Supplemental Identifiers

RxCUI
979480 979485 979492
UPC
0331722702300 0331722700900 0331722701303
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 ANDA203835 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (31722-702-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (31722-702-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (31722-702-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (31722-702-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (31722-702-90)
source: ndc

Packages (5)

31722-702-05 500 TABLET, FILM COATED in 1 BOTTLE (31722-702-05) 31722-702-10 1000 TABLET, FILM COATED in 1 BOTTLE (31722-702-10) 31722-702-30 30 TABLET, FILM COATED in 1 BOTTLE (31722-702-30) 31722-702-60 60 TABLET, FILM COATED in 1 BOTTLE (31722-702-60) 31722-702-90 90 TABLET, FILM COATED in 1 BOTTLE (31722-702-90)

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": "40b34aeb-20b5-4200-e063-6394a90a96e9", "openfda": {"upc": ["0331722702300", "0331722700900", "0331722701303"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["cafd54e8-42a8-474c-8ea8-49ec74c2b0d3"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-702-05)", "package_ndc": "31722-702-05", "marketing_start_date": "20150819"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (31722-702-10)", "package_ndc": "31722-702-10", "marketing_start_date": "20150819"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-702-30)", "package_ndc": "31722-702-30", "marketing_start_date": "20150819"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (31722-702-60)", "package_ndc": "31722-702-60", "marketing_start_date": "20150819"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-702-90)", "package_ndc": "31722-702-90", "marketing_start_date": "20150819"}], "brand_name": "Losartan Potassium", "product_id": "31722-702_40b34aeb-20b5-4200-e063-6394a90a96e9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "31722-702", "generic_name": "Losartan Potassium", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20261231"}