Package 63323-089-50

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 63323-089-50
Digits Only 6332308950
Product NDC 63323-089
Product ID 63323-089_9def795c-abcf-483c-8b1d-e4374666efb2
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (63323-089-50) / 50 mL in 1 VIAL, SINGLE-DOSE (63323-089-25)

Marketing

Marketing Status
Marketed Since 2025-08-25
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": "9def795c-abcf-483c-8b1d-e4374666efb2", "openfda": {"upc": ["0363323089252", "0363323083038"], "unii": ["8MDF5V39QO"], "rxcui": ["1868469", "1868486"], "spl_set_id": ["0ab55004-bb63-436d-ad77-cd3796905370"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (63323-089-50)  / 50 mL in 1 VIAL, SINGLE-DOSE (63323-089-25)", "package_ndc": "63323-089-50", "marketing_start_date": "20250825"}], "brand_name": "Sodium Bicarbonate", "product_id": "63323-089_9def795c-abcf-483c-8b1d-e4374666efb2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "63323-089", "generic_name": "Sodium Bicarbonate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA206688", "marketing_category": "ANDA", "marketing_start_date": "20250825", "listing_expiration_date": "20261231"}