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 20 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-635
Product ID 71610-635_e9231c86-1596-42eb-b1f8-61747c75f030
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076796
Listing Expiration 2026-12-31
Marketing Start 2022-01-04

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 71610635
Hyphenated Format 71610-635

Supplemental Identifiers

RxCUI
197732 310429 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
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71610-635-30)
  • 45 TABLET in 1 BOTTLE (71610-635-45)
  • 60 TABLET in 1 BOTTLE (71610-635-53)
  • 90 TABLET in 1 BOTTLE (71610-635-60)
  • 180 TABLET in 1 BOTTLE (71610-635-80)
  • 270 TABLET in 1 BOTTLE (71610-635-92)
source: ndc

Packages (6)

71610-635-30 30 TABLET in 1 BOTTLE (71610-635-30) 71610-635-45 45 TABLET in 1 BOTTLE (71610-635-45) 71610-635-53 60 TABLET in 1 BOTTLE (71610-635-53) 71610-635-60 90 TABLET in 1 BOTTLE (71610-635-60) 71610-635-80 180 TABLET in 1 BOTTLE (71610-635-80) 71610-635-92 270 TABLET in 1 BOTTLE (71610-635-92)

Ingredients (1)

furosemide (20 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": "e9231c86-1596-42eb-b1f8-61747c75f030", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "310429", "313988"], "spl_set_id": ["6f124d7d-a19d-4de6-8ea4-719a42eb520b"], "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 (71610-635-30)", "package_ndc": "71610-635-30", "marketing_start_date": "20220222"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71610-635-45)", "package_ndc": "71610-635-45", "marketing_start_date": "20220308"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71610-635-53)", "package_ndc": "71610-635-53", "marketing_start_date": "20220222"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-635-60)", "package_ndc": "71610-635-60", "marketing_start_date": "20220222"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71610-635-80)", "package_ndc": "71610-635-80", "marketing_start_date": "20220222"}, {"sample": false, "description": "270 TABLET in 1 BOTTLE (71610-635-92)", "package_ndc": "71610-635-92", "marketing_start_date": "20220222"}], "brand_name": "Furosemide", "product_id": "71610-635_e9231c86-1596-42eb-b1f8-61747c75f030", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "71610-635", "generic_name": "furosemide", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20220104", "listing_expiration_date": "20261231"}