Package 51407-612-90

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 51407-612-90
Digits Only 5140761290
Product NDC 51407-612
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-612-90)

Marketing

Marketing Status
Marketed Since 2022-01-27
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": "14d2de37-621a-5030-e063-6294a90a8632", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["d6aae78e-308b-7072-e053-2a95a90aaa10"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (51407-612-90)", "package_ndc": "51407-612-90", "marketing_start_date": "20220127"}], "brand_name": "Pantoprazole Sodium", "product_id": "51407-612_14d2de37-621a-5030-e063-6294a90a8632", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "51407-612", "generic_name": "Pantoprazole Sodium", "labeler_name": "Golden State Medical Supply, 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"}