Package 62175-618-43

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 62175-618-43
Digits Only 6217561843
Product NDC 62175-618
Description

1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-618-43)

Marketing

Marketing Status
Marketed Since 2011-01-20
Brand pantoprazole sodium
Generic pantoprazole sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cfbf12d8-f656-4b99-bd2e-fb11bab669e5", "openfda": {"upc": ["0362175617460", "0362175180469"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["e7705bf6-e473-4b9c-bb5d-57e26ffe7b97"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-618-43)", "package_ndc": "62175-618-43", "marketing_start_date": "20110120"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-618-46)", "package_ndc": "62175-618-46", "marketing_start_date": "20110120"}], "brand_name": "Pantoprazole Sodium", "product_id": "62175-618_cfbf12d8-f656-4b99-bd2e-fb11bab669e5", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "62175-618", "generic_name": "Pantoprazole Sodium", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA078281", "marketing_category": "ANDA", "marketing_start_date": "20110120", "listing_expiration_date": "20261231"}