Package 55154-4236-5

Brand: protonix i.v.

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 55154-4236-5
Digits Only 5515442365
Product NDC 55154-4236
Description

5 VIAL in 1 CARTON (55154-4236-5) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2001-05-01
Brand protonix i.v.
Generic pantoprazole sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "435bdafe-e862-45bf-8432-bcb56944009f", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669", "885257"], "spl_set_id": ["50802e19-72d3-4130-8d14-eb94361b38e7"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (55154-4236-5)  / 10 mL in 1 VIAL", "package_ndc": "55154-4236-5", "marketing_start_date": "20010501"}], "brand_name": "Protonix I.V.", "product_id": "55154-4236_435bdafe-e862-45bf-8432-bcb56944009f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "55154-4236", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Protonix", "brand_name_suffix": "I.V.", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/10mL"}], "application_number": "NDA020988", "marketing_category": "NDA", "marketing_start_date": "20010501", "listing_expiration_date": "20261231"}