Package 60760-646-30

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 60760-646-30
Digits Only 6076064630
Product NDC 60760-646
Product ID 60760-646_e8815323-26a9-4f59-e053-2995a90ab690
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-646-30)

Marketing

Marketing Status
Marketed Since 2022-08-25
Brand pantoprazole sodium
Generic pantoprazole sodium
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": "e8815323-26a9-4f59-e053-2995a90ab690", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["e8816b1f-2f29-b26e-e053-2a95a90a92f3"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-646-30)", "package_ndc": "60760-646-30", "marketing_start_date": "20220825"}], "brand_name": "Pantoprazole Sodium", "product_id": "60760-646_e8815323-26a9-4f59-e053-2995a90ab690", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "60760-646", "generic_name": "Pantoprazole Sodium", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA202038", "marketing_category": "ANDA", "marketing_start_date": "20220825", "listing_expiration_date": "20261231"}