Package 60760-712-60

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 60760-712-60
Digits Only 6076071260
Product NDC 60760-712
Product ID 60760-712_292d7c25-a31a-8eef-e063-6394a90a99a1
Description

60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-712-60)

Marketing

Marketing Status
Marketed Since 2020-03-04
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": "292d7c25-a31a-8eef-e063-6394a90a99a1", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872"], "spl_set_id": ["a0341042-1a55-73f6-e053-2a95a90a5b1b"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-712-60)", "package_ndc": "60760-712-60", "marketing_start_date": "20200304"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "60760-712_292d7c25-a31a-8eef-e063-6394a90a99a1", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "60760-712", "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": "20 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_start_date": "20200304", "listing_expiration_date": "20261231"}