furosemide

Generic: furosemide

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

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler precision dose inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

furosemide 40 mg/4mL

Manufacturer
Precision Dose Inc.

Identifiers & Regulatory

Product NDC 68094-756
Product ID 68094-756_2a35f26b-d831-48a5-ab87-14c61f0341bf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070434
Listing Expiration 2026-12-31
Marketing Start 2012-10-23

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 68094756
Hyphenated Format 68094-756

Supplemental Identifiers

RxCUI
197730
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 ANDA070434 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/4mL
source: ndc
Packaging
  • 3 TRAY in 1 CASE (68094-756-62) / 10 CUP, UNIT-DOSE in 1 TRAY / 4 mL in 1 CUP, UNIT-DOSE (68094-756-59)
source: ndc

Packages (1)

Ingredients (1)

furosemide (40 mg/4mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a35f26b-d831-48a5-ab87-14c61f0341bf", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197730"], "spl_set_id": ["4a746634-379b-4847-a965-7607d2a71bed"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Precision Dose Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "3 TRAY in 1 CASE (68094-756-62)  / 10 CUP, UNIT-DOSE in 1 TRAY / 4 mL in 1 CUP, UNIT-DOSE (68094-756-59)", "package_ndc": "68094-756-62", "marketing_start_date": "20121023"}], "brand_name": "Furosemide", "product_id": "68094-756_2a35f26b-d831-48a5-ab87-14c61f0341bf", "dosage_form": "SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "68094-756", "generic_name": "Furosemide", "labeler_name": "Precision Dose Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/4mL"}], "application_number": "ANDA070434", "marketing_category": "ANDA", "marketing_start_date": "20121023", "listing_expiration_date": "20261231"}