Package 63323-530-75

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 63323-530-75
Digits Only 6332353075
Product NDC 63323-530
Product ID 63323-530_613e9aef-5e01-4d00-8407-488872b9902f
Description

20 BAG in 1 CASE (63323-530-75) / 500 mL in 1 BAG (63323-530-21)

Marketing

Marketing Status
Marketed Since 2020-03-20
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": "613e9aef-5e01-4d00-8407-488872b9902f", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["730781"], "spl_set_id": ["51da05ce-e3c4-4ef5-a845-dc869152e17f"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BAG in 1 CASE (63323-530-75)  / 500 mL in 1 BAG (63323-530-21)", "package_ndc": "63323-530-75", "marketing_start_date": "20200320"}], "brand_name": "Sodium Chloride", "product_id": "63323-530_613e9aef-5e01-4d00-8407-488872b9902f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "63323-530", "generic_name": "Sodium Chloride", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "3 g/100mL"}], "application_number": "ANDA209476", "marketing_category": "ANDA", "marketing_start_date": "20200320", "listing_expiration_date": "20261231"}