Package 0404-9951-05

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 0404-9951-05
Digits Only 0404995105
Product NDC 0404-9951
Product ID 0404-9951_1cc6a0c6-0475-4c98-92ab-a6184974cfd7
Description

1 VIAL, SINGLE-USE in 1 BAG (0404-9951-05) / 5 mL in 1 VIAL, SINGLE-USE

Marketing

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

Linked Drug Pages (1)

SODIUM BICARBONATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "1cc6a0c6-0475-4c98-92ab-a6184974cfd7", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868469"], "spl_set_id": ["da484a2f-154f-48b4-8467-7a86729204c3"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 BAG (0404-9951-05)  / 5 mL in 1 VIAL, SINGLE-USE", "package_ndc": "0404-9951-05", "marketing_start_date": "20220112"}], "brand_name": "SODIUM BICARBONATE", "product_id": "0404-9951_1cc6a0c6-0475-4c98-92ab-a6184974cfd7", "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": "0404-9951", "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": "42 mg/mL"}], "application_number": "ANDA202981", "marketing_category": "ANDA", "marketing_start_date": "20220112", "listing_expiration_date": "20261231"}