Package 13668-096-90

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 13668-096-90
Digits Only 1366809690
Product NDC 13668-096
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (13668-096-90)

Marketing

Marketing Status
Marketed Since 2011-01-20
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": "7d09300f-2078-458c-9328-f83ffd997c9e", "openfda": {"upc": ["0313668096903", "0313668429305"], "unii": ["6871619Q5X"], "rxcui": ["251872", "314200"], "spl_set_id": ["9c983da1-a8e0-479e-8816-5d5668ea242e"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (13668-096-90)", "package_ndc": "13668-096-90", "marketing_start_date": "20110120"}], "brand_name": "Pantoprazole Sodium", "product_id": "13668-096_7d09300f-2078-458c-9328-f83ffd997c9e", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "13668-096", "generic_name": "Pantoprazole Sodium", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA090074", "marketing_category": "ANDA", "marketing_start_date": "20110120", "listing_expiration_date": "20271231"}