Package 82009-011-90

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 82009-011-90
Digits Only 8200901190
Product NDC 82009-011
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (82009-011-90)

Marketing

Marketing Status
Marketed Since 2022-06-06
Brand pantoprazole sodium
Generic pantoprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48430767-cec0-15e0-e063-6394a90ac032", "openfda": {"upc": ["0382009010908", "0382009011905"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["643eb498-d916-4fb7-9281-32895575ab36"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (82009-011-10)", "package_ndc": "82009-011-10", "marketing_start_date": "20220606"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (82009-011-90)", "package_ndc": "82009-011-90", "marketing_start_date": "20220606"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "82009-011_48430767-cec0-15e0-e063-6394a90ac032", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "82009-011", "generic_name": "PANTOPRAZOLE", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20220606", "listing_expiration_date": "20271231"}