furosemide

Generic: furosemide

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

Drug Facts

Product Profile

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

furosemide 20 mg/1

Manufacturer
Prefferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8870
Product ID 68788-8870_ede9846b-b4c5-4be2-9188-fd65e66cd893
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216629
Listing Expiration 2026-12-31
Marketing Start 2025-04-30

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 687888870
Hyphenated Format 68788-8870

Supplemental Identifiers

RxCUI
310429
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 ANDA216629 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-8870-1)
  • 30 TABLET in 1 BOTTLE (68788-8870-3)
  • 60 TABLET in 1 BOTTLE (68788-8870-6)
  • 90 TABLET in 1 BOTTLE (68788-8870-9)
source: ndc

Packages (4)

68788-8870-1 100 TABLET in 1 BOTTLE (68788-8870-1) 68788-8870-3 30 TABLET in 1 BOTTLE (68788-8870-3) 68788-8870-6 60 TABLET in 1 BOTTLE (68788-8870-6) 68788-8870-9 90 TABLET in 1 BOTTLE (68788-8870-9)

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": "ede9846b-b4c5-4be2-9188-fd65e66cd893", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["ede9846b-b4c5-4be2-9188-fd65e66cd893"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Prefferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8870-1)", "package_ndc": "68788-8870-1", "marketing_start_date": "20250430"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8870-3)", "package_ndc": "68788-8870-3", "marketing_start_date": "20250430"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8870-6)", "package_ndc": "68788-8870-6", "marketing_start_date": "20250430"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8870-9)", "package_ndc": "68788-8870-9", "marketing_start_date": "20250430"}], "brand_name": "Furosemide", "product_id": "68788-8870_ede9846b-b4c5-4be2-9188-fd65e66cd893", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "68788-8870", "generic_name": "Furosemide", "labeler_name": "Prefferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA216629", "marketing_category": "ANDA", "marketing_start_date": "20250430", "listing_expiration_date": "20261231"}