Package 72789-086-30

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 72789-086-30
Digits Only 7278908630
Product NDC 72789-086
Product ID 72789-086_4031c357-7001-521b-e063-6294a90a232c
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-086-30)

Marketing

Marketing Status
Marketed Since 2020-06-04
Brand pantoprazole sodium
Generic pantoprazole sodium
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": "4031c357-7001-521b-e063-6294a90a232c", "openfda": {"upc": ["0372789086309"], "unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["b422c5eb-9a6d-4f8c-863d-ca515ec780c2"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-086-30)", "package_ndc": "72789-086-30", "marketing_start_date": "20200604"}], "brand_name": "Pantoprazole Sodium", "product_id": "72789-086_4031c357-7001-521b-e063-6294a90a232c", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72789-086", "generic_name": "Pantoprazole Sodium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA078281", "marketing_category": "ANDA", "marketing_start_date": "20110120", "listing_expiration_date": "20261231"}