pantoprazole sodium

Generic: pantoprazole sodium

Labeler: mckesson corporation dba sky packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler mckesson corporation dba sky packaging
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
McKesson Corporation dba SKY Packaging

Identifiers & Regulatory

Product NDC 63739-564
Product ID 63739-564_2f9bfd2f-129e-a52a-e063-6294a90a9856
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078281
Marketing Start 2011-01-20
Marketing End 2026-04-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63739564
Hyphenated Format 63739-564

Supplemental Identifiers

RxCUI
314200
UNII
6871619Q5X

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 ANDA078281 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-564-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

63739-564-10 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-564-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK

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": "2f9bfd2f-129e-a52a-e063-6294a90a9856", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["a0141135-3f83-49ba-b50c-31f353bf42f4"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-564-10)  / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "63739-564-10", "marketing_end_date": "20260430", "marketing_start_date": "20110120"}], "brand_name": "Pantoprazole Sodium", "product_id": "63739-564_2f9bfd2f-129e-a52a-e063-6294a90a9856", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "63739-564", "generic_name": "Pantoprazole Sodium", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA078281", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20110120"}