furosemide

Generic: furosemide

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 40 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-049
Product ID 71610-049_780ad204-2238-4c8b-b477-7c93a6b53781
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076796
Listing Expiration 2026-12-31
Marketing Start 2004-03-26

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 71610049
Hyphenated Format 71610-049

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 ANDA076796 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (71610-049-30)
  • 45 TABLET in 1 BOTTLE, PLASTIC (71610-049-45)
  • 60 TABLET in 1 BOTTLE, PLASTIC (71610-049-53)
  • 90 TABLET in 1 BOTTLE, PLASTIC (71610-049-60)
  • 180 TABLET in 1 BOTTLE, PLASTIC (71610-049-80)
source: ndc

Packages (5)

71610-049-30 30 TABLET in 1 BOTTLE, PLASTIC (71610-049-30) 71610-049-45 45 TABLET in 1 BOTTLE, PLASTIC (71610-049-45) 71610-049-53 60 TABLET in 1 BOTTLE, PLASTIC (71610-049-53) 71610-049-60 90 TABLET in 1 BOTTLE, PLASTIC (71610-049-60) 71610-049-80 180 TABLET in 1 BOTTLE, PLASTIC (71610-049-80)

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": "780ad204-2238-4c8b-b477-7c93a6b53781", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["1d2733ac-6fa6-44d1-96d4-f1a698045ad2"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71610-049-30)", "package_ndc": "71610-049-30", "marketing_start_date": "20180416"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE, PLASTIC (71610-049-45)", "package_ndc": "71610-049-45", "marketing_start_date": "20180416"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (71610-049-53)", "package_ndc": "71610-049-53", "marketing_start_date": "20180416"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71610-049-60)", "package_ndc": "71610-049-60", "marketing_start_date": "20180416"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (71610-049-80)", "package_ndc": "71610-049-80", "marketing_start_date": "20180416"}], "brand_name": "Furosemide", "product_id": "71610-049_780ad204-2238-4c8b-b477-7c93a6b53781", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "71610-049", "generic_name": "furosemide", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}