Package 51754-5012-4

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 51754-5012-4
Digits Only 5175450124
Product NDC 51754-5012
Product ID 51754-5012_4da0ba66-756d-4b4d-8018-81ca16578ef1
Description

25 VIAL in 1 CARTON (51754-5012-4) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2018-09-27
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": "4da0ba66-756d-4b4d-8018-81ca16578ef1", "openfda": {"unii": ["8MDF5V39QO"], "rxcui": ["807284", "1868486", "1923484", "2198792"], "spl_set_id": ["e9698a4f-1a95-4f28-a945-e8009d1d6dd4"], "manufacturer_name": ["Exela Pharma Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (51754-5012-4)  / 10 mL in 1 VIAL", "package_ndc": "51754-5012-4", "marketing_start_date": "20180927"}], "brand_name": "Sodium Bicarbonate", "product_id": "51754-5012_4da0ba66-756d-4b4d-8018-81ca16578ef1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "51754-5012", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Exela Pharma Sciences, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "42 mg/mL"}], "application_number": "ANDA211091", "marketing_category": "ANDA", "marketing_start_date": "20180927", "listing_expiration_date": "20261231"}