torsemide

Generic: torsemide

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

Drug Facts

Product Profile

Brand Name torsemide
Generic Name torsemide
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

torsemide 20 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-531
Product ID 31722-531_4ee76b17-e459-457b-b67a-bb062a408150
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079234
Listing Expiration 2026-12-31
Marketing Start 2011-01-01

Pharmacologic Class

Established (EPC)
loop diuretic [epc]
Physiologic Effect
increased diuresis at loop of henle [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722531
Hyphenated Format 31722-531

Supplemental Identifiers

RxCUI
198369 198370 198371 198372
UPC
0331722529013 0331722531016 0331722530019 0331722532013
UNII
W31X2H97FB
NUI
N0000175366 N0000175590

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 torsemide (source: ndc)
Generic Name torsemide (source: ndc)
Application Number ANDA079234 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (31722-531-01)
  • 500 TABLET in 1 BOTTLE (31722-531-05)
source: ndc

Packages (2)

31722-531-01 100 TABLET in 1 BOTTLE (31722-531-01) 31722-531-05 500 TABLET in 1 BOTTLE (31722-531-05)

Ingredients (1)

torsemide (20 mg/1)

Linked Drug Pages (1)

Torsemide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4ee76b17-e459-457b-b67a-bb062a408150", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0331722529013", "0331722531016", "0331722530019", "0331722532013"], "unii": ["W31X2H97FB"], "rxcui": ["198369", "198370", "198371", "198372"], "spl_set_id": ["0d4a4ef9-0944-452c-b014-bd822bfb9dd9"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-531-01)", "package_ndc": "31722-531-01", "marketing_start_date": "20110101"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-531-05)", "package_ndc": "31722-531-05", "marketing_start_date": "20110101"}], "brand_name": "Torsemide", "product_id": "31722-531_4ee76b17-e459-457b-b67a-bb062a408150", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "31722-531", "generic_name": "Torsemide", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Torsemide", "active_ingredients": [{"name": "TORSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA079234", "marketing_category": "ANDA", "marketing_start_date": "20110101", "listing_expiration_date": "20261231"}