pantoprazole sodium

Generic: pantoprazole sodium

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

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

pantoprazole sodium 40 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9284
Product ID 0143-9284_284915b9-082e-4c76-8998-13aff7221045
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA209463
Listing Expiration 2026-12-31
Marketing Start 2017-09-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439284
Hyphenated Format 0143-9284

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 (0143-9284-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9284-01)
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": "284915b9-082e-4c76-8998-13aff7221045", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["b02f3f85-8f9b-4d06-8eae-73e592626f3e"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9284-10)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9284-01)", "package_ndc": "0143-9284-10", "marketing_start_date": "20170922"}], "brand_name": "Pantoprazole Sodium", "product_id": "0143-9284_284915b9-082e-4c76-8998-13aff7221045", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "0143-9284", "generic_name": "Pantoprazole Sodium", "labeler_name": "Hikma Pharmaceuticals USA 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": "20170922", "listing_expiration_date": "20261231"}