Package 68071-2285-6

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 68071-2285-6
Digits Only 6807122856
Product NDC 68071-2285
Product ID 68071-2285_1d783072-b076-e384-e063-6394a90a7460
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2285-6)

Marketing

Marketing Status
Marketed Since 2020-10-27
Brand pantoprazole sodium
Generic pantoprazole
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": "1d783072-b076-e384-e063-6394a90a7460", "openfda": {"upc": ["0368071228564"], "unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["b2abc159-e450-99dc-e053-2a95a90abe6a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2285-6)", "package_ndc": "68071-2285-6", "marketing_start_date": "20201027"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "68071-2285_1d783072-b076-e384-e063-6394a90a7460", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68071-2285", "generic_name": "PANTOPRAZOLE", "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": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20261231"}