furosemide

Generic: furosemide

Labeler: maiva pharma private limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler maiva pharma private limited
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
Maiva Pharma Private Limited

Identifiers & Regulatory

Product NDC 73542-101
Product ID 73542-101_dddc74d0-e63a-431b-a222-12c45bdc0c16
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203428
Listing Expiration 2026-12-31
Marketing Start 2025-06-16

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 73542101
Hyphenated Format 73542-101

Supplemental Identifiers

RxCUI
1719286 1719290 1719291
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 ANDA203428 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (73542-101-25) / 2 mL in 1 VIAL
source: ndc

Packages (1)

73542-101-25 25 VIAL in 1 CARTON (73542-101-25) / 2 mL in 1 VIAL

Ingredients (1)

furosemide (10 mg/mL)

Linked Drug Pages (1)

Furosemide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "dddc74d0-e63a-431b-a222-12c45bdc0c16", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["e5880bf4-5037-4813-b7cc-656a6832ecb5"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Maiva Pharma Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (73542-101-25)  / 2 mL in 1 VIAL", "package_ndc": "73542-101-25", "marketing_start_date": "20250616"}], "brand_name": "Furosemide", "product_id": "73542-101_dddc74d0-e63a-431b-a222-12c45bdc0c16", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "73542-101", "generic_name": "Furosemide", "labeler_name": "Maiva Pharma Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA203428", "marketing_category": "ANDA", "marketing_start_date": "20250616", "listing_expiration_date": "20261231"}