Package 68645-596-54

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 68645-596-54
Digits Only 6864559654
Product NDC 68645-596
Product ID 68645-596_4743c756-8182-70d4-e063-6294a90abc4f
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (68645-596-54)

Marketing

Marketing Status
Marketed Since 2014-09-10
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": "4743c756-8182-70d4-e063-6294a90abc4f", "openfda": {"upc": ["0368645596549"], "unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["de0f3767-9dba-4de7-e053-2a95a90aa3c6"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68645-596-54)", "package_ndc": "68645-596-54", "marketing_start_date": "20140910"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "68645-596_4743c756-8182-70d4-e063-6294a90abc4f", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68645-596", "generic_name": "PANTOPRAZOLE", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "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"}