pantoprazole sodium

Generic: pantoprazole sodium

Labeler: sun pharmaceutical industries limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

pantoprazole sodium 40 mg/10mL

Manufacturer
Sun Pharmaceutical Industries Limited

Identifiers & Regulatory

Product NDC 70095-024
Product ID 70095-024_b423abbc-01e1-4d07-9c89-a7398c898d2f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204400
Listing Expiration 2026-12-31
Marketing Start 2023-04-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70095024
Hyphenated Format 70095-024

Supplemental Identifiers

RxCUI
283669
UPC
0370095024039
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 CARTON in 1 PACKAGE (70095-024-02) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01)
  • 25 CARTON in 1 PACKAGE (70095-024-03) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01)
source: ndc

Packages (2)

70095-024-02 10 CARTON in 1 PACKAGE (70095-024-02) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01) 70095-024-03 25 CARTON in 1 PACKAGE (70095-024-03) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01)

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": "b423abbc-01e1-4d07-9c89-a7398c898d2f", "openfda": {"upc": ["0370095024039"], "unii": ["6871619Q5X"], "rxcui": ["283669"], "spl_set_id": ["eb3f58d4-0c69-4377-be45-c36099c98d33"], "manufacturer_name": ["Sun Pharmaceutical Industries Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTON in 1 PACKAGE (70095-024-02)  / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01)", "package_ndc": "70095-024-02", "marketing_start_date": "20230403"}, {"sample": false, "description": "25 CARTON in 1 PACKAGE (70095-024-03)  / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01)", "package_ndc": "70095-024-03", "marketing_start_date": "20230403"}], "brand_name": "Pantoprazole sodium", "product_id": "70095-024_b423abbc-01e1-4d07-9c89-a7398c898d2f", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "70095-024", "generic_name": "Pantoprazole sodium", "labeler_name": "Sun Pharmaceutical Industries Limited", "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": "20230403", "listing_expiration_date": "20261231"}