pantoprazole sodium

Generic: pantoprazole sodium

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler aurobindo pharma limited
Dosage Form GRANULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-671
Product ID 59651-671_b3cec41e-e98b-470a-8ba2-c31537023989
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217923
Listing Expiration 2026-12-31
Marketing Start 2025-03-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651671
Hyphenated Format 59651-671

Supplemental Identifiers

RxCUI
763306
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 ANDA217923 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 PACKET in 1 CARTON (59651-671-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET
source: ndc

Packages (1)

59651-671-30 30 PACKET in 1 CARTON (59651-671-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET

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": ["ORAL"], "spl_id": "b3cec41e-e98b-470a-8ba2-c31537023989", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["763306"], "spl_set_id": ["b3cec41e-e98b-470a-8ba2-c31537023989"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 PACKET in 1 CARTON (59651-671-30)  / 1 GRANULE, DELAYED RELEASE in 1 PACKET", "package_ndc": "59651-671-30", "marketing_start_date": "20250331"}], "brand_name": "PANTOPRAZOLE SODIUM", "product_id": "59651-671_b3cec41e-e98b-470a-8ba2-c31537023989", "dosage_form": "GRANULE, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "59651-671", "generic_name": "PANTOPRAZOLE SODIUM", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANTOPRAZOLE SODIUM", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA217923", "marketing_category": "ANDA", "marketing_start_date": "20250331", "listing_expiration_date": "20261231"}