Package 60760-679-30

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 60760-679-30
Digits Only 6076067930
Product NDC 60760-679
Product ID 60760-679_e1aa611e-7960-a074-e053-2a95a90a914e
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-679-30)

Marketing

Marketing Status
Marketed Since 2022-03-01
Brand pantoprazole sodium
Generic pantoprazole
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": "e1aa611e-7960-a074-e053-2a95a90a914e", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["e1aa55ec-5e0e-3a58-e053-2a95a90abe4f"], "manufacturer_name": ["St Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-679-30)", "package_ndc": "60760-679-30", "marketing_start_date": "20220301"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "60760-679_e1aa611e-7960-a074-e053-2a95a90a914e", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "60760-679", "generic_name": "PANTOPRAZOLE", "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": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20220301", "listing_expiration_date": "20261231"}