furosemide

Generic: furosemide

Labeler: lifestar pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler lifestar pharma llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
Lifestar Pharma LLC

Identifiers & Regulatory

Product NDC 70756-619
Product ID 70756-619_d4f07f52-c316-401b-b852-a1b29e3570b8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216860
Listing Expiration 2026-12-31
Marketing Start 2022-12-17

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 70756619
Hyphenated Format 70756-619

Supplemental Identifiers

RxCUI
1719286 1719290 1719291
UPC
0370756619857 0370756618829 0370756620860
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 ANDA216860 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 5 VIAL in 1 CARTON (70756-619-05) / 4 mL in 1 VIAL (70756-619-85)
  • 10 VIAL in 1 CARTON (70756-619-10) / 4 mL in 1 VIAL (70756-619-85)
  • 25 VIAL in 1 CARTON (70756-619-25) / 4 mL in 1 VIAL (70756-619-85)
source: ndc

Packages (3)

70756-619-05 5 VIAL in 1 CARTON (70756-619-05) / 4 mL in 1 VIAL (70756-619-85) 70756-619-10 10 VIAL in 1 CARTON (70756-619-10) / 4 mL in 1 VIAL (70756-619-85) 70756-619-25 25 VIAL in 1 CARTON (70756-619-25) / 4 mL in 1 VIAL (70756-619-85)

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": "d4f07f52-c316-401b-b852-a1b29e3570b8", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0370756619857", "0370756618829", "0370756620860"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["92f3ab5d-361c-4e12-bb50-fd4a9f195a8f"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (70756-619-05)  / 4 mL in 1 VIAL (70756-619-85)", "package_ndc": "70756-619-05", "marketing_start_date": "20221217"}, {"sample": false, "description": "10 VIAL in 1 CARTON (70756-619-10)  / 4 mL in 1 VIAL (70756-619-85)", "package_ndc": "70756-619-10", "marketing_start_date": "20221217"}, {"sample": false, "description": "25 VIAL in 1 CARTON (70756-619-25)  / 4 mL in 1 VIAL (70756-619-85)", "package_ndc": "70756-619-25", "marketing_start_date": "20221217"}], "brand_name": "Furosemide", "product_id": "70756-619_d4f07f52-c316-401b-b852-a1b29e3570b8", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70756-619", "generic_name": "furosemide", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA216860", "marketing_category": "ANDA", "marketing_start_date": "20221217", "listing_expiration_date": "20261231"}