Package 68071-2215-4

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 68071-2215-4
Digits Only 6807122154
Product NDC 68071-2215
Description

14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2215-4)

Marketing

Marketing Status
Marketed Since 2020-07-08
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": "23838cc7-f093-d306-e063-6394a90a1647", "openfda": {"upc": ["0368071221541"], "unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["a9f32edf-e0b9-4e96-e053-2a95a90afbc8"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2215-3)", "package_ndc": "68071-2215-3", "marketing_start_date": "20200708"}, {"sample": false, "description": "14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2215-4)", "package_ndc": "68071-2215-4", "marketing_start_date": "20200708"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "68071-2215_23838cc7-f093-d306-e063-6394a90a1647", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68071-2215", "generic_name": "PANTOPRAZOLE", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20140910", "listing_expiration_date": "20261231"}