Package 72603-177-01

Brand: pantoprazole

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 72603-177-01
Digits Only 7260317701
Product NDC 72603-177
Product ID 72603-177_57338853-6995-de1e-62ca-be5505c8d656
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-177-01)

Marketing

Marketing Status
Marketed Since 2023-12-15
Brand pantoprazole
Generic pantoprazole
Sample Package No

Linked Drug Pages (1)

Pantoprazole ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "57338853-6995-de1e-62ca-be5505c8d656", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["82f0103a-2b97-d210-6d7d-c627d60ad694"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (72603-177-01)", "package_ndc": "72603-177-01", "marketing_start_date": "20231215"}], "brand_name": "Pantoprazole", "product_id": "72603-177_57338853-6995-de1e-62ca-be5505c8d656", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72603-177", "generic_name": "Pantoprazole", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA077619", "marketing_category": "ANDA", "marketing_start_date": "20231215", "listing_expiration_date": "20261231"}