Package 0409-6660-75

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 0409-6660-75
Digits Only 0409666075
Product NDC 0409-6660
Product ID 0409-6660_c9a3fd1e-32d2-4aa7-bbb4-2852e5c71c8d
Description

25 VIAL in 1 TRAY (0409-6660-75) / 40 mL in 1 VIAL (0409-6660-01)

Marketing

Marketing Status
Marketed Since 2005-07-29
Brand sodium chloride
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

Sodium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c9a3fd1e-32d2-4aa7-bbb4-2852e5c71c8d", "openfda": {"unii": ["451W47IQ8X"], "spl_set_id": ["018a8807-1331-41c3-4889-c7ec502a9043"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (0409-6660-75)  / 40 mL in 1 VIAL (0409-6660-01)", "package_ndc": "0409-6660-75", "marketing_start_date": "20050729"}], "brand_name": "Sodium Chloride", "product_id": "0409-6660_c9a3fd1e-32d2-4aa7-bbb4-2852e5c71c8d", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0409-6660", "generic_name": "SODIUM CHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "5.84 g/40mL"}], "application_number": "NDA018897", "marketing_category": "NDA", "marketing_start_date": "20050729", "listing_expiration_date": "20271231"}