Package 72789-268-30

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 72789-268-30
Digits Only 7278926830
Product NDC 72789-268
Product ID 72789-268_4bad4f9b-8b65-9a6d-e063-6294a90a8930
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-268-30)

Marketing

Marketing Status
Marketed Since 2022-08-12
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": "4bad4f9b-8b65-9a6d-e063-6294a90a8930", "openfda": {"upc": ["0372789268309"], "unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["c1f37929-a981-4ace-95e6-ae6795a797b3"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-268-30)", "package_ndc": "72789-268-30", "marketing_start_date": "20220812"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "72789-268_4bad4f9b-8b65-9a6d-e063-6294a90a8930", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72789-268", "generic_name": "PANTOPRAZOLE", "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": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20140910", "listing_expiration_date": "20271231"}