Package 72189-112-30

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 72189-112-30
Digits Only 7218911230
Product NDC 72189-112
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-30)

Marketing

Marketing Status
Marketed Since 2020-06-12
Brand pantoprazole sodium
Generic pantoprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2be8f6ba-3289-86ab-e063-6394a90acb89", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["a7e7c1ab-3e75-1ff8-e053-2995a90a7539"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-30)", "package_ndc": "72189-112-30", "marketing_start_date": "20200612"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-60)", "package_ndc": "72189-112-60", "marketing_start_date": "20200612"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-90)", "package_ndc": "72189-112-90", "marketing_start_date": "20200612"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "72189-112_2be8f6ba-3289-86ab-e063-6394a90acb89", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72189-112", "generic_name": "pantoprazole", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20200612", "listing_expiration_date": "20261231"}