torsemide

Generic: torsemide

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name torsemide
Generic Name torsemide
Labeler avkare
Dosage Form TABLET
Routes
ORAL
Active Ingredients

torsemide 20 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 42291-818
Product ID 42291-818_4a94f559-d26f-5817-e063-6294a90ab408
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076346
Listing Expiration 2027-12-31
Marketing Start 2017-04-03

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 42291818
Hyphenated Format 42291-818

Supplemental Identifiers

RxCUI
198369 198370 198371 198372
UNII
W31X2H97FB
NUI
N0000175366 N0000175590

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 ANDA076346 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (42291-818-01)
  • 500 TABLET in 1 BOTTLE (42291-818-50)
  • 90 TABLET in 1 BOTTLE (42291-818-90)
source: ndc

Packages (3)

Ingredients (1)

torsemide (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a94f559-d26f-5817-e063-6294a90ab408", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["W31X2H97FB"], "rxcui": ["198369", "198370", "198371", "198372"], "spl_set_id": ["7fc14338-92e4-cf57-a3e8-ef64d8d1026c"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42291-818-01)", "package_ndc": "42291-818-01", "marketing_start_date": "20230315"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (42291-818-50)", "package_ndc": "42291-818-50", "marketing_start_date": "20230315"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-818-90)", "package_ndc": "42291-818-90", "marketing_start_date": "20170403"}], "brand_name": "Torsemide", "product_id": "42291-818_4a94f559-d26f-5817-e063-6294a90ab408", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "42291-818", "generic_name": "Torsemide", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Torsemide", "active_ingredients": [{"name": "TORSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA076346", "marketing_category": "ANDA", "marketing_start_date": "20170403", "listing_expiration_date": "20271231"}