pantoprazole sodium i.v. (0781-3480)

Drug Facts

Product Profile

Brand Name pantoprazole sodium i.v.

Generic Name pantoprazole sodium

Labeler sandoz inc

Dosage Form INJECTION, POWDER, FOR SOLUTION

Routes

INTRAVENOUS

Active Ingredients

pantoprazole sodium 40 mg/10mL

Manufacturer

Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-3480

Product ID 0781-3480_38e9f0e0-9691-4c5d-b4aa-d3d314df242c

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA209524

Listing Expiration 2027-12-31

Marketing Start 2026-01-26

Pharmacologic Class

Classes

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07813480

Hyphenated Format 0781-3480

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 i.v. (source: ndc)

Generic Name pantoprazole sodium (source: ndc)

Application Number ANDA209524 (source: ndc)

Routes

INTRAVENOUS

source: ndc

Resolved Composition

Strengths

40 mg/10mL

source: ndc

Packaging

10 VIAL in 1 CARTON (0781-3480-95) / 10 mL in 1 VIAL

source: ndc

Packages (1)

0781-3480-95 10 VIAL in 1 CARTON (0781-3480-95) / 10 mL in 1 VIAL

Ingredients (1)

pantoprazole sodium (40 mg/10mL)

Linked Drug Pages (1)

PANTOPRAZOLE SODIUM I.V. ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["INTRAVENOUS"], "spl_id": "38e9f0e0-9691-4c5d-b4aa-d3d314df242c", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["22b71a1d-87f8-43ba-b53d-53ca3f70c63e"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0781-3480-95)  / 10 mL in 1 VIAL", "package_ndc": "0781-3480-95", "marketing_start_date": "20260126"}], "brand_name": "PANTOPRAZOLE SODIUM I.V.", "product_id": "0781-3480_38e9f0e0-9691-4c5d-b4aa-d3d314df242c", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0781-3480", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "brand_name_suffix": "I.V.", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/10mL"}], "application_number": "ANDA209524", "marketing_category": "ANDA", "marketing_start_date": "20260126", "listing_expiration_date": "20271231"}