furosemide

Generic: furosemide

Labeler: micro labs limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler micro labs limited
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

furosemide 40 mg/4mL

Manufacturer
Micro Labs Limited

Identifiers & Regulatory

Product NDC 42571-437
Product ID 42571-437_4829e889-87d2-9d87-e063-6294a90a11cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218188
Listing Expiration 2027-12-31
Marketing Start 2023-11-16

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 42571437
Hyphenated Format 42571-437

Supplemental Identifiers

RxCUI
1719286 1719290 1719291
UPC
0342571437862 0342571438562 0342571436759
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 ANDA218188 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/4mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (42571-437-66) / 4 mL in 1 VIAL (42571-437-86)
source: ndc

Packages (1)

42571-437-66 25 VIAL in 1 CARTON (42571-437-66) / 4 mL in 1 VIAL (42571-437-86)

Ingredients (1)

furosemide (40 mg/4mL)

Linked Drug Pages (1)

Furosemide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4829e889-87d2-9d87-e063-6294a90a11cb", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0342571437862", "0342571438562", "0342571436759"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["2f547f7c-0322-465c-9764-43f955d98ab2"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (42571-437-66)  / 4 mL in 1 VIAL (42571-437-86)", "package_ndc": "42571-437-66", "marketing_start_date": "20231116"}], "brand_name": "Furosemide", "product_id": "42571-437_4829e889-87d2-9d87-e063-6294a90a11cb", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "42571-437", "generic_name": "Furosemide", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/4mL"}], "application_number": "ANDA218188", "marketing_category": "ANDA", "marketing_start_date": "20231116", "listing_expiration_date": "20271231"}