furosemide

Generic: furosemide

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-030
Product ID 72789-030_3c6c8aa2-377c-0261-e063-6294a90a066b
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 72789030
Hyphenated Format 72789-030

Supplemental Identifiers

RxCUI
310429
UPC
0372789030302
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, PLASTIC (72789-030-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-030-60)
source: ndc

Packages (2)

72789-030-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-030-30) 72789-030-60 60 TABLET in 1 BOTTLE, PLASTIC (72789-030-60)

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": "3c6c8aa2-377c-0261-e063-6294a90a066b", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0372789030302"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["c24489c3-65e0-44e3-a50a-8bb0672e8821"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-030-30)", "package_ndc": "72789-030-30", "marketing_start_date": "20191205"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-030-60)", "package_ndc": "72789-030-60", "marketing_start_date": "20191205"}], "brand_name": "Furosemide", "product_id": "72789-030_3c6c8aa2-377c-0261-e063-6294a90a066b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72789-030", "generic_name": "furosemide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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": "20040326", "listing_expiration_date": "20261231"}