pantoprazole sodium
Generic: pantoprazole
Labeler: quality care products, llcDrug Facts
Product Profile
Brand Name
pantoprazole sodium
Generic Name
pantoprazole
Labeler
quality care products, llc
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
pantoprazole sodium 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55700-850
Product ID
55700-850_2e409a27-bc0c-4d4a-bd5a-fa93f4a5265d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202882
Marketing Start
2020-03-20
Marketing End
2026-04-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55700850
Hyphenated Format
55700-850
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
pantoprazole sodium (source: ndc)
Generic Name
pantoprazole (source: ndc)
Application Number
ANDA202882 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-850-30)
Packages (1)
Ingredients (1)
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"}