furosemide

Generic: furosemide

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6646
Product ID 50090-6646_012b9271-9cc3-467a-8542-d519d59e27a9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216629
Listing Expiration 2027-12-31
Marketing Start 2022-11-05

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 500906646
Hyphenated Format 50090-6646

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 ANDA216629 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-6646-0)
  • 100 TABLET in 1 BOTTLE (50090-6646-1)
  • 60 TABLET in 1 BOTTLE (50090-6646-3)
  • 90 TABLET in 1 BOTTLE (50090-6646-9)
source: ndc

Packages (4)

Ingredients (1)

furosemide (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "012b9271-9cc3-467a-8542-d519d59e27a9", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["8f56d6f6-a5ea-4171-9e24-d2fdb11a65f8"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6646-0)", "package_ndc": "50090-6646-0", "marketing_start_date": "20230829"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-6646-1)", "package_ndc": "50090-6646-1", "marketing_start_date": "20230829"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-6646-3)", "package_ndc": "50090-6646-3", "marketing_start_date": "20230829"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6646-9)", "package_ndc": "50090-6646-9", "marketing_start_date": "20230829"}], "brand_name": "Furosemide", "product_id": "50090-6646_012b9271-9cc3-467a-8542-d519d59e27a9", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-6646", "generic_name": "Furosemide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA216629", "marketing_category": "ANDA", "marketing_start_date": "20221105", "listing_expiration_date": "20271231"}