Package 70121-1164-5

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 70121-1164-5
Digits Only 7012111645
Product NDC 70121-1164
Description

25 VIAL, GLASS in 1 CARTON (70121-1164-5) / 4 mL in 1 VIAL, GLASS (70121-1164-1)

Marketing

Marketing Status
Marketed Since 2016-07-25
Brand furosemide
Generic furosemide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0243d363-b856-4a4a-a160-a691ca8c6621", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0370121107613", "0370121107651", "0370121116356", "0370121116417", "0370121116318", "0370121116455"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["d5b9f12e-d1e9-42de-90f2-c9ba33a86457"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, GLASS in 1 CARTON (70121-1164-5)  / 4 mL in 1 VIAL, GLASS (70121-1164-1)", "package_ndc": "70121-1164-5", "marketing_start_date": "20160725"}], "brand_name": "Furosemide", "product_id": "70121-1164_0243d363-b856-4a4a-a160-a691ca8c6621", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70121-1164", "generic_name": "Furosemide", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/4mL"}], "application_number": "ANDA207552", "marketing_category": "ANDA", "marketing_start_date": "20160725", "listing_expiration_date": "20261231"}