Package 0990-7972-08

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 0990-7972-08
Digits Only 0990797208
Product NDC 0990-7972
Description

4 POUCH in 1 CASE (0990-7972-08) / 1 BAG in 1 POUCH / 3000 mL in 1 BAG

Marketing

Marketing Status
Marketed Since 2019-07-01
Brand sodium chloride
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["IRRIGATION"], "spl_id": "8e1ca6c4-2e03-4c2f-b69b-be57bb896c1c", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["486515"], "spl_set_id": ["009bef3c-e8ac-46be-b564-a2556adf0081"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 POUCH in 1 CASE (0990-7972-08)  / 1 BAG in 1 POUCH / 3000 mL in 1 BAG", "package_ndc": "0990-7972-08", "marketing_start_date": "20190701"}], "brand_name": "Sodium Chloride", "product_id": "0990-7972_8e1ca6c4-2e03-4c2f-b69b-be57bb896c1c", "dosage_form": "IRRIGANT", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0990-7972", "generic_name": "SODIUM CHLORIDE", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "900 mg/100mL"}], "application_number": "NDA018314", "marketing_category": "NDA", "marketing_start_date": "20190701", "listing_expiration_date": "20261231"}