Package 68071-5053-6

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 68071-5053-6
Digits Only 6807150536
Product NDC 68071-5053
Product ID 68071-5053_1b42fa33-63a2-2c69-e063-6294a90a043e
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-5053-6)

Marketing

Marketing Status
Marketed Since 2019-09-11
Brand pantoprazole sodium
Generic pantoprazole sodium
Sample Package No

Linked Drug Pages (1)

Pantoprazole Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1b42fa33-63a2-2c69-e063-6294a90a043e", "openfda": {"upc": ["0368071505368"], "unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["924a80b9-de48-90c0-e053-2995a90a00e1"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-5053-6)", "package_ndc": "68071-5053-6", "marketing_start_date": "20190911"}], "brand_name": "Pantoprazole Sodium", "product_id": "68071-5053_1b42fa33-63a2-2c69-e063-6294a90a043e", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68071-5053", "generic_name": "Pantoprazole Sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20120928", "listing_expiration_date": "20261231"}