Package 68071-3524-3

Brand: pantoprazole

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 68071-3524-3
Digits Only 6807135243
Product NDC 68071-3524
Product ID 68071-3524_2d3f76b4-d1b8-0d4a-e063-6294a90ac5f9
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3524-3)

Marketing

Marketing Status
Marketed Since 2023-10-18
Brand pantoprazole
Generic pantoprazole
Sample Package No

Linked Drug Pages (1)

Pantoprazole ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d3f76b4-d1b8-0d4a-e063-6294a90ac5f9", "openfda": {"upc": ["0368071352436"], "unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["07ff83f9-7039-ac26-e063-6394a90a37ce"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3524-3)", "package_ndc": "68071-3524-3", "marketing_start_date": "20231018"}], "brand_name": "Pantoprazole", "product_id": "68071-3524_2d3f76b4-d1b8-0d4a-e063-6294a90ac5f9", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68071-3524", "generic_name": "Pantoprazole", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA077619", "marketing_category": "ANDA", "marketing_start_date": "20110119", "listing_expiration_date": "20261231"}