Package 51079-051-20
Brand: pantoprazole sodium
Generic: pantoprazole sodiumPackage Facts
Identity
Package NDC
51079-051-20
Digits Only
5107905120
Product NDC
51079-051
Description
100 BLISTER PACK in 1 CARTON (51079-051-20) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (51079-051-01)
Marketing
Marketing Status
Brand
pantoprazole sodium
Generic
pantoprazole sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a875ad3-8a73-b446-e063-6294a90a1a63", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["a9b0d279-118b-4372-bd51-d4bad9c1cfca"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-051-20) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (51079-051-01)", "package_ndc": "51079-051-20", "marketing_start_date": "20110223"}], "brand_name": "Pantoprazole Sodium", "product_id": "51079-051_3a875ad3-8a73-b446-e063-6294a90a1a63", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "51079-051", "generic_name": "pantoprazole sodium", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA090970", "marketing_category": "ANDA", "marketing_start_date": "20110223", "listing_expiration_date": "20261231"}