Package 55700-850-30

Brand: pantoprazole sodium

Generic: pantoprazole
NDC Package

Package Facts

Identity

Package NDC 55700-850-30
Digits Only 5570085030
Product NDC 55700-850
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-850-30)

Marketing

Marketing Status
Discontinued 2026-04-30
Brand pantoprazole sodium
Generic pantoprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e409a27-bc0c-4d4a-bd5a-fa93f4a5265d", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["65098903-ccb5-4daf-ab1b-d9823fc73066"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-850-30)", "package_ndc": "55700-850-30", "marketing_end_date": "20260430", "marketing_start_date": "20200320"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "55700-850_2e409a27-bc0c-4d4a-bd5a-fa93f4a5265d", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "55700-850", "generic_name": "PANTOPRAZOLE", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA202882", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20200320"}