Package 60760-574-30

Brand: pantoprazole

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 60760-574-30
Digits Only 6076057430
Product NDC 60760-574
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-574-30)

Marketing

Marketing Status
Marketed Since 2023-08-29
Brand pantoprazole
Generic pantoprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45381395-cf3f-23fe-e063-6394a90a13df", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["ed264262-21bb-1bae-e053-2995a90a8a5e"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-574-30)", "package_ndc": "60760-574-30", "marketing_start_date": "20230829"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-574-60)", "package_ndc": "60760-574-60", "marketing_start_date": "20221031"}], "brand_name": "Pantoprazole", "product_id": "60760-574_45381395-cf3f-23fe-e063-6394a90a13df", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "60760-574", "generic_name": "Pantoprazole", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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": "20221031", "listing_expiration_date": "20261231"}