Package 72572-740-25

Brand: sodium bicarbonate

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 72572-740-25
Digits Only 7257274025
Product NDC 72572-740
Product ID 72572-740_8fcbd37e-e4d5-4137-9abf-c398fbb5cbf0
Description

25 VIAL in 1 CARTON (72572-740-25) / 50 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2024-02-01
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": "8fcbd37e-e4d5-4137-9abf-c398fbb5cbf0", "openfda": {"upc": ["0372572740258"], "unii": ["8MDF5V39QO"], "rxcui": ["1868486"], "spl_set_id": ["a10fdfbc-94a0-49ab-b26c-de1df042bc89"], "manufacturer_name": ["Civica"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72572-740-25)  / 50 mL in 1 VIAL", "package_ndc": "72572-740-25", "marketing_start_date": "20240201"}], "brand_name": "Sodium Bicarbonate", "product_id": "72572-740_8fcbd37e-e4d5-4137-9abf-c398fbb5cbf0", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Alkalinizing Activity [MoA]"], "product_ndc": "72572-740", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Civica", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Bicarbonate", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "84 mg/mL"}], "application_number": "ANDA211091", "marketing_category": "ANDA", "marketing_start_date": "20190801", "listing_expiration_date": "20261231"}