Package 0409-5555-02

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 0409-5555-02
Digits Only 0409555502
Product NDC 0409-5555
Product ID 0409-5555_037c4aeb-4a95-4c37-8214-a30110b1d47f
Description

25 VIAL, SINGLE-USE in 1 TRAY (0409-5555-02) / 5 mL in 1 VIAL, SINGLE-USE (0409-5555-12)

Marketing

Marketing Status
Marketed Since 2019-10-21
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": "037c4aeb-4a95-4c37-8214-a30110b1d47f", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["1868469"], "spl_set_id": ["ea9f4498-0d43-4043-8dd1-f22537841c21"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-USE in 1 TRAY (0409-5555-02)  / 5 mL in 1 VIAL, SINGLE-USE (0409-5555-12)", "package_ndc": "0409-5555-02", "marketing_start_date": "20191021"}], "brand_name": "Sodium Bicarbonate", "product_id": "0409-5555_037c4aeb-4a95-4c37-8214-a30110b1d47f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "0409-5555", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Hospira, 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": "20191021", "listing_expiration_date": "20261231"}