Package 0404-9980-50

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 0404-9980-50
Digits Only 0404998050
Product NDC 0404-9980
Description

1 VIAL, SINGLE-DOSE in 1 BAG (0404-9980-50) / 50 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-01-12
Brand sodium bicarbonate
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f4b91a27-936d-417e-adb4-905b14e91bc1", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["ea9ad1a6-84f2-44d8-bf93-fb8f3d3fce9c"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9980-50)  / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9980-50", "marketing_start_date": "20220112"}], "brand_name": "Sodium Bicarbonate", "product_id": "0404-9980_f4b91a27-936d-417e-adb4-905b14e91bc1", "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": "0404-9980", "generic_name": "sodium bicarbonate", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20220112", "listing_expiration_date": "20261231"}