Package 72572-553-10

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 72572-553-10
Digits Only 7257255310
Product NDC 72572-553
Description

10 VIAL in 1 CARTON (72572-553-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (72572-553-01)

Marketing

Marketing Status
Marketed Since 2025-06-01
Brand pantoprazole sodium
Generic pantoprazole sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9d6f752f-428f-455d-8f09-3b74c68524fb", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["c857dc41-7b47-4f26-a9f5-d76eb82b44ee"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (72572-553-10)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (72572-553-01)", "package_ndc": "72572-553-10", "marketing_start_date": "20250601"}], "brand_name": "Pantoprazole Sodium", "product_id": "72572-553_9d6f752f-428f-455d-8f09-3b74c68524fb", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72572-553", "generic_name": "Pantoprazole Sodium", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "NDA209463", "marketing_category": "NDA", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}