pantoprazole sodium

Generic: pantoprazole sodium

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

pantoprazole sodium 40 mg/10mL

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-129
Product ID 62756-129_ef1bb9ed-b534-4698-abf5-836dcce85f45
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077674
Listing Expiration 2026-12-31
Marketing Start 2019-09-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756129
Hyphenated Format 62756-129

Supplemental Identifiers

RxCUI
283669
UPC
0362756129405
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 ANDA077674 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/10mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (62756-129-40) / 10 mL in 1 VIAL
  • 10 VIAL in 1 CARTON (62756-129-44) / 10 mL in 1 VIAL
  • 25 CARTON in 1 PACKAGE (62756-129-45) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL
source: ndc

Packages (3)

62756-129-40 1 VIAL in 1 CARTON (62756-129-40) / 10 mL in 1 VIAL 62756-129-44 10 VIAL in 1 CARTON (62756-129-44) / 10 mL in 1 VIAL 62756-129-45 25 CARTON in 1 PACKAGE (62756-129-45) / 1 VIAL in 1 CARTON / 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": "ef1bb9ed-b534-4698-abf5-836dcce85f45", "openfda": {"upc": ["0362756129405"], "unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["d9fcf6a2-3788-4955-84d9-3c319b13267c"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (62756-129-40)  / 10 mL in 1 VIAL", "package_ndc": "62756-129-40", "marketing_start_date": "20190901"}, {"sample": false, "description": "10 VIAL in 1 CARTON (62756-129-44)  / 10 mL in 1 VIAL", "package_ndc": "62756-129-44", "marketing_start_date": "20190901"}, {"sample": false, "description": "25 CARTON in 1 PACKAGE (62756-129-45)  / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL", "package_ndc": "62756-129-45", "marketing_start_date": "20190901"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "62756-129_ef1bb9ed-b534-4698-abf5-836dcce85f45", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "62756-129", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/10mL"}], "application_number": "ANDA077674", "marketing_category": "ANDA", "marketing_start_date": "20190901", "listing_expiration_date": "20261231"}