Package 0008-0923-60

Brand: protonix i.v.

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 0008-0923-60
Digits Only 0008092360
Product NDC 0008-0923
Description

25 CARTON in 1 PACKAGE (0008-0923-60) / 1 VIAL in 1 CARTON / 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": "a7e7d657-a748-4234-8dd6-c0e4d0f81a86", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669", "885257"], "spl_set_id": ["51e4144a-489e-436c-609a-39305f8f56ba"], "manufacturer_name": ["Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0008-0923-51)  / 10 mL in 1 VIAL", "package_ndc": "0008-0923-51", "marketing_start_date": "20010501"}, {"sample": false, "description": "10 CARTON in 1 PACKAGE (0008-0923-55)  / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL", "package_ndc": "0008-0923-55", "marketing_start_date": "20010501"}, {"sample": false, "description": "25 CARTON in 1 PACKAGE (0008-0923-60)  / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL", "package_ndc": "0008-0923-60", "marketing_start_date": "20010501"}], "brand_name": "Protonix I.V.", "product_id": "0008-0923_a7e7d657-a748-4234-8dd6-c0e4d0f81a86", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0008-0923", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.", "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"}