Package 68071-4864-9

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 68071-4864-9
Digits Only 6807148649
Product NDC 68071-4864
Product ID 68071-4864_1ae1b6c2-d5e4-1029-e063-6394a90a5d6a
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4864-9)

Marketing

Marketing Status
Marketed Since 2019-04-24
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": "1ae1b6c2-d5e4-1029-e063-6394a90a5d6a", "openfda": {"upc": ["0368071486490"], "unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["8748a588-a1e5-9dfc-e053-2a95a90a846c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4864-9)", "package_ndc": "68071-4864-9", "marketing_start_date": "20190424"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "68071-4864_1ae1b6c2-d5e4-1029-e063-6394a90a5d6a", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68071-4864", "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"}