Package 68071-4895-9

Brand: pantoprazole sodium

Generic: pantoprazole sodium
NDC Package

Package Facts

Identity

Package NDC 68071-4895-9
Digits Only 6807148959
Product NDC 68071-4895
Product ID 68071-4895_1ae22ca4-77dd-fb33-e063-6294a90a8f77
Description

90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4895-9)

Marketing

Marketing Status
Marketed Since 2019-05-15
Brand pantoprazole sodium
Generic pantoprazole sodium
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": "1ae22ca4-77dd-fb33-e063-6294a90a8f77", "openfda": {"upc": ["0368071489590"], "unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["88f408cf-1b3e-4d7a-e053-2a95a90a369f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4895-9)", "package_ndc": "68071-4895-9", "marketing_start_date": "20190515"}], "brand_name": "Pantoprazole Sodium", "product_id": "68071-4895_1ae22ca4-77dd-fb33-e063-6294a90a8f77", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "68071-4895", "generic_name": "Pantoprazole Sodium", "labeler_name": "NuCare Pharmaceuticals,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": "20120928", "listing_expiration_date": "20261231"}