furosemide

Generic: furosemide

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

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 40 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-0251
Product ID 70518-0251_47e58bf6-e13d-346e-e063-6294a90a690c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077293
Listing Expiration 2027-12-31
Marketing Start 2017-02-22

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 705180251
Hyphenated Format 70518-0251

Supplemental Identifiers

RxCUI
313988
UNII
7LXU5N7ZO5
NUI
N0000175366 N0000175590

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 ANDA077293 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-0251-1)
  • 100 TABLET in 1 BOTTLE, PLASTIC (70518-0251-2)
  • 30 TABLET in 1 BLISTER PACK (70518-0251-3)
source: ndc

Packages (3)

70518-0251-1 90 TABLET in 1 BOTTLE, PLASTIC (70518-0251-1) 70518-0251-2 100 TABLET in 1 BOTTLE, PLASTIC (70518-0251-2) 70518-0251-3 30 TABLET in 1 BLISTER PACK (70518-0251-3)

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": "47e58bf6-e13d-346e-e063-6294a90a690c", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["916de29e-228c-4dfc-bcee-ad9a641316bd"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-0251-1)", "package_ndc": "70518-0251-1", "marketing_start_date": "20170317"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-0251-2)", "package_ndc": "70518-0251-2", "marketing_start_date": "20170421"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0251-3)", "package_ndc": "70518-0251-3", "marketing_start_date": "20180410"}], "brand_name": "Furosemide", "product_id": "70518-0251_47e58bf6-e13d-346e-e063-6294a90a690c", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70518-0251", "generic_name": "Furosemide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20170222", "listing_expiration_date": "20271231"}