pantoprazole sodium

Generic: pantoprazole sodium

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler sagent pharmaceuticals
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

pantoprazole sodium 40 mg/10mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-751
Product ID 25021-751_2b04a735-571c-4668-bc78-ac3a611d575c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204400
Listing Expiration 2026-12-31
Marketing Start 2022-07-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021751
Hyphenated Format 25021-751

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 ANDA204400 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/10mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (25021-751-10) / 10 mL in 1 VIAL
  • 25 VIAL in 1 CARTON (25021-751-11) / 10 mL in 1 VIAL
source: ndc

Packages (2)

25021-751-10 10 VIAL in 1 CARTON (25021-751-10) / 10 mL in 1 VIAL 25021-751-11 25 VIAL in 1 CARTON (25021-751-11) / 10 mL in 1 VIAL

Ingredients (1)

pantoprazole sodium (40 mg/10mL)

Linked Drug Pages (1)

Pantoprazole Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "2b04a735-571c-4668-bc78-ac3a611d575c", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["c39be14b-e881-4586-b77e-4747db494954"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-751-10)  / 10 mL in 1 VIAL", "package_ndc": "25021-751-10", "marketing_start_date": "20220715"}, {"sample": false, "description": "25 VIAL in 1 CARTON (25021-751-11)  / 10 mL in 1 VIAL", "package_ndc": "25021-751-11", "marketing_start_date": "20220715"}], "brand_name": "Pantoprazole Sodium", "product_id": "25021-751_2b04a735-571c-4668-bc78-ac3a611d575c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "25021-751", "generic_name": "Pantoprazole Sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/10mL"}], "application_number": "ANDA204400", "marketing_category": "ANDA", "marketing_start_date": "20220715", "listing_expiration_date": "20261231"}