pantoprazole sodium
Generic: pantoprazole sodium
Labeler: civica, inc.Drug Facts
Product Profile
Brand Name
pantoprazole sodium
Generic Name
pantoprazole sodium
Labeler
civica, inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
pantoprazole sodium 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72572-553
Product ID
72572-553_9d6f752f-428f-455d-8f09-3b74c68524fb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA209463
Listing Expiration
2026-12-31
Marketing Start
2025-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72572553
Hyphenated Format
72572-553
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 sodium (source: ndc)
Application Number
NDA209463 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 10 VIAL in 1 CARTON (72572-553-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (72572-553-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9d6f752f-428f-455d-8f09-3b74c68524fb", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["c857dc41-7b47-4f26-a9f5-d76eb82b44ee"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (72572-553-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (72572-553-01)", "package_ndc": "72572-553-10", "marketing_start_date": "20250601"}], "brand_name": "Pantoprazole Sodium", "product_id": "72572-553_9d6f752f-428f-455d-8f09-3b74c68524fb", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "72572-553", "generic_name": "Pantoprazole Sodium", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "NDA209463", "marketing_category": "NDA", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}