pantoprazole sodium

Generic: pantoprazole sodium

Labeler: civica, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler civica, inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
Civica, Inc.

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
proton pump inhibitor [epc] proton pump inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72572553
Hyphenated Format 72572-553

Supplemental Identifiers

RxCUI
283669
UNII
6871619Q5X

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (72572-553-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (72572-553-01)
source: ndc

Packages (1)

Ingredients (1)

pantoprazole sodium (40 mg/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"}