furosemide

Generic: furosemide

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler redpharm drug
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2136
Product ID 67296-2136_46aca8aa-d9cd-f44a-e063-6294a90aef3e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216629
Listing Expiration 2026-12-31
Marketing Start 2022-11-05

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 672962136
Hyphenated Format 67296-2136

Supplemental Identifiers

RxCUI
310429
UPC
0364980564014
UNII
7LXU5N7ZO5
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 furosemide (source: ndc)
Generic Name furosemide (source: ndc)
Application Number ANDA216629 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (67296-2136-3)
source: ndc

Packages (1)

67296-2136-3 30 TABLET in 1 BOTTLE (67296-2136-3)

Ingredients (1)

furosemide (20 mg/1)

Linked Drug Pages (1)

Furosemide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "46aca8aa-d9cd-f44a-e063-6294a90aef3e", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0364980564014"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["37457273-38a1-f938-e063-6294a90a50ab"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-2136-3)", "package_ndc": "67296-2136-3", "marketing_start_date": "20221105"}], "brand_name": "Furosemide", "product_id": "67296-2136_46aca8aa-d9cd-f44a-e063-6294a90aef3e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "67296-2136", "generic_name": "Furosemide", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA216629", "marketing_category": "ANDA", "marketing_start_date": "20221105", "listing_expiration_date": "20261231"}