Package 72162-2367-5

Brand: rabeprazole sodium

Generic: rabeprazole sodium
NDC Package

Package Facts

Identity

Package NDC 72162-2367-5
Digits Only 7216223675
Product NDC 72162-2367
Product ID 72162-2367_52e17eb4-6cf4-4516-a04b-2859262f7fbb
Description

500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2367-5)

Marketing

Marketing Status
Marketed Since 2024-07-16
Brand rabeprazole sodium
Generic rabeprazole sodium
Sample Package No

Linked Drug Pages (1)

Rabeprazole Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "52e17eb4-6cf4-4516-a04b-2859262f7fbb", "openfda": {"unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["8d8c1a72-b4c4-4699-b9c3-3a39a9df44f2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2367-5)", "package_ndc": "72162-2367-5", "marketing_start_date": "20240716"}], "brand_name": "Rabeprazole Sodium", "product_id": "72162-2367_52e17eb4-6cf4-4516-a04b-2859262f7fbb", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72162-2367", "generic_name": "Rabeprazole Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rabeprazole Sodium", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA208644", "marketing_category": "ANDA", "marketing_start_date": "20180427", "listing_expiration_date": "20261231"}