Package 71288-600-92

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 71288-600-92
Digits Only 7128860092
Product NDC 71288-600
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (71288-600-92) / 10 mL in 1 VIAL, SINGLE-DOSE (71288-600-91)

Marketing

Marketing Status
Marketed Since 2022-08-29
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": "48bbc577-3242-4da3-bca3-7a5f89105415", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["014f9762-6948-46b7-8659-5c89f35ad8bf"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (71288-600-92)  / 10 mL in 1 VIAL, SINGLE-DOSE (71288-600-91)", "package_ndc": "71288-600-92", "marketing_start_date": "20220829"}], "brand_name": "Pantoprazole Sodium", "product_id": "71288-600_48bbc577-3242-4da3-bca3-7a5f89105415", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "71288-600", "generic_name": "Pantoprazole Sodium", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/10mL"}], "application_number": "ANDA215860", "marketing_category": "ANDA", "marketing_start_date": "20220829", "listing_expiration_date": "20261231"}