furosemide

Generic: furosemide

Labeler: meitheal pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler meitheal pharmaceuticals inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
Meitheal Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 71288-203
Product ID 71288-203_53a09c30-7295-4337-89a4-93d3748d6ea3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212803
Listing Expiration 2026-12-31
Marketing Start 2022-01-27

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 71288203
Hyphenated Format 71288-203

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 ANDA212803 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-92) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-203-91)
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-94) / 10 mL in 1 VIAL, SINGLE-DOSE (71288-203-93)
source: ndc

Packages (2)

71288-203-92 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-92) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-203-91) 71288-203-94 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-94) / 10 mL in 1 VIAL, SINGLE-DOSE (71288-203-93)

Ingredients (1)

furosemide (10 mg/mL)

Linked Drug Pages (2)

Furosemide ndc-match (0.9) Furosemide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "53a09c30-7295-4337-89a4-93d3748d6ea3", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["3aadaca7-3661-4bfe-87f8-6368e4ab6536"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-92)  / 2 mL in 1 VIAL, SINGLE-DOSE (71288-203-91)", "package_ndc": "71288-203-92", "marketing_start_date": "20220127"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (71288-203-94)  / 10 mL in 1 VIAL, SINGLE-DOSE (71288-203-93)", "package_ndc": "71288-203-94", "marketing_start_date": "20220127"}], "brand_name": "Furosemide", "product_id": "71288-203_53a09c30-7295-4337-89a4-93d3748d6ea3", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "71288-203", "generic_name": "Furosemide", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA212803", "marketing_category": "ANDA", "marketing_start_date": "20220127", "listing_expiration_date": "20261231"}