furosemide

Generic: furosemide

Labeler: ipca laboratories limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler ipca laboratories limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 40 mg/1

Manufacturer
Ipca Laboratories Limited

Identifiers & Regulatory

Product NDC 83980-003
Product ID 83980-003_2ef79eb1-61e5-4697-9292-336ca5cf5116
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078010
Listing Expiration 2026-12-31
Marketing Start 2024-06-03

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 83980003
Hyphenated Format 83980-003

Supplemental Identifiers

RxCUI
197732 310429 313988
UPC
0383980004016 0383980003019 0383980002012
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 ANDA078010 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (83980-003-01)
  • 1000 TABLET in 1 BOTTLE (83980-003-10)
  • 10 TABLET in 1 BOTTLE (83980-003-97)
source: ndc

Packages (3)

83980-003-01 100 TABLET in 1 BOTTLE (83980-003-01) 83980-003-10 1000 TABLET in 1 BOTTLE (83980-003-10) 83980-003-97 10 TABLET in 1 BOTTLE (83980-003-97)

Ingredients (1)

furosemide (40 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": "2ef79eb1-61e5-4697-9292-336ca5cf5116", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0383980004016", "0383980003019", "0383980002012"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "310429", "313988"], "spl_set_id": ["0acd293b-ecab-4879-a8e7-cd1b76148f2a"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Ipca Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (83980-003-01)", "package_ndc": "83980-003-01", "marketing_start_date": "20240603"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (83980-003-10)", "package_ndc": "83980-003-10", "marketing_start_date": "20240603"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (83980-003-97)", "package_ndc": "83980-003-97", "marketing_start_date": "20240603"}], "brand_name": "Furosemide", "product_id": "83980-003_2ef79eb1-61e5-4697-9292-336ca5cf5116", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "83980-003", "generic_name": "Furosemide", "labeler_name": "Ipca Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA078010", "marketing_category": "ANDA", "marketing_start_date": "20240603", "listing_expiration_date": "20261231"}