Package 50268-639-15

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 50268-639-15
Digits Only 5026863915
Product NDC 50268-639
Description

50 BLISTER PACK in 1 BOX (50268-639-15) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (50268-639-11)

Marketing

Marketing Status
Marketed Since 2015-02-19
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": "47fb0652-007e-e12b-e063-6294a90ab81a", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["dcac4022-fea1-67c5-3331-fefcc3c440d8"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-639-15)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (50268-639-11)", "package_ndc": "50268-639-15", "marketing_start_date": "20150219"}], "brand_name": "Pantoprazole Sodium", "product_id": "50268-639_47fb0652-007e-e12b-e063-6294a90ab81a", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "50268-639", "generic_name": "Pantoprazole Sodium", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA078281", "marketing_category": "ANDA", "marketing_start_date": "20150219", "listing_expiration_date": "20271231"}