pantoprazole sodium

Generic: pantoprazole sodium

Labeler: eugia us llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler eugia us llc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
Eugia US LLC

Identifiers & Regulatory

Product NDC 55150-202
Product ID 55150-202_7de2a288-9f73-44ec-a42d-ea76d1018645
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205675
Listing Expiration 2026-12-31
Marketing Start 2016-03-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55150202
Hyphenated Format 55150-202

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 ANDA205675 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00)
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00)
source: ndc

Packages (2)

55150-202-10 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00) 55150-202-25 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00)

Ingredients (1)

pantoprazole sodium (40 mg/1)

Linked Drug Pages (1)

Pantoprazole Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "7de2a288-9f73-44ec-a42d-ea76d1018645", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["9bed093a-9586-4c82-a2b7-c68f89d0faef"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-10)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00)", "package_ndc": "55150-202-10", "marketing_start_date": "20160330"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-25)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00)", "package_ndc": "55150-202-25", "marketing_start_date": "20160330"}], "brand_name": "Pantoprazole Sodium", "product_id": "55150-202_7de2a288-9f73-44ec-a42d-ea76d1018645", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "55150-202", "generic_name": "Pantoprazole Sodium", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA205675", "marketing_category": "ANDA", "marketing_start_date": "20160330", "listing_expiration_date": "20261231"}