Package 70518-0860-0

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 70518-0860-0
Digits Only 7051808600
Product NDC 70518-0860
Product ID 70518-0860_4845be9c-3ccf-00d8-e063-6394a90aacfd
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0860-0)

Marketing

Marketing Status
Marketed Since 2017-11-20
Brand pantoprazole sodium
Generic pantoprazole sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4845be9c-3ccf-00d8-e063-6394a90aacfd", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["f313159c-115a-4cf6-b32e-9ddc833fd51c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0860-0)", "package_ndc": "70518-0860-0", "marketing_start_date": "20171120"}], "brand_name": "Pantoprazole Sodium", "product_id": "70518-0860_4845be9c-3ccf-00d8-e063-6394a90aacfd", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "70518-0860", "generic_name": "Pantoprazole Sodium", "labeler_name": "REMEDYREPACK INC.", "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": "20171120", "listing_expiration_date": "20271231"}