furosemide

Generic: furosemide

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-753
Product ID 62135-753_31443d9b-3dee-5aa9-e063-6294a90adcfd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018413
Listing Expiration 2026-12-31
Marketing Start 1983-11-30

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 62135753
Hyphenated Format 62135-753

Supplemental Identifiers

RxCUI
310429 313988
UPC
0362135754907 0362135753900
UNII
7LXU5N7ZO5
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 furosemide (source: ndc)
Generic Name furosemide (source: ndc)
Application Number NDA018413 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 PACKAGE (62135-753-90)
source: ndc

Packages (1)

62135-753-90 90 TABLET in 1 PACKAGE (62135-753-90)

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": "31443d9b-3dee-5aa9-e063-6294a90adcfd", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0362135754907", "0362135753900"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429", "313988"], "spl_set_id": ["8ebd2f10-acfc-48a4-a5db-f20377bda9ce"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 PACKAGE (62135-753-90)", "package_ndc": "62135-753-90", "marketing_start_date": "20240417"}], "brand_name": "Furosemide", "product_id": "62135-753_31443d9b-3dee-5aa9-e063-6294a90adcfd", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "62135-753", "generic_name": "Furosemide", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "NDA018413", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19831130", "listing_expiration_date": "20261231"}