Package 36000-064-05

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 36000-064-05
Digits Only 3600006405
Product NDC 36000-064
Description

5 VIAL, SINGLE-DOSE in 1 BOX (36000-064-05) / 4 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2014-02-06
Brand furosemide
Generic furosemide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b4c1ae97-0f6c-4ae1-858a-4e0ab8f1ce53", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0336000063012", "0336000065016", "0336000283250", "0336000282253", "0336000064019", "0336000284257"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["c71371a7-75c5-45b8-b762-8d782d4c71bc"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL, SINGLE-DOSE in 1 BOX (36000-064-05)  / 4 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "36000-064-05", "marketing_start_date": "20140206"}], "brand_name": "FUROSEMIDE", "product_id": "36000-064_b4c1ae97-0f6c-4ae1-858a-4e0ab8f1ce53", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "36000-064", "generic_name": "furosemide", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FUROSEMIDE", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA202747", "marketing_category": "ANDA", "marketing_start_date": "20140206", "listing_expiration_date": "20261231"}