pantoprazole sodium

Generic: pantoprazole sodium

Labeler: mylan institutional inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pantoprazole sodium
Generic Name pantoprazole sodium
Labeler mylan institutional inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

pantoprazole sodium 40 mg/1

Manufacturer
Mylan Institutional Inc.

Identifiers & Regulatory

Product NDC 51079-051
Product ID 51079-051_3a875ad3-8a73-b446-e063-6294a90a1a63
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090970
Listing Expiration 2026-12-31
Marketing Start 2011-02-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51079051
Hyphenated Format 51079-051

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 ANDA090970 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (51079-051-20) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (51079-051-01)
source: ndc

Packages (1)

Ingredients (1)

pantoprazole sodium (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a875ad3-8a73-b446-e063-6294a90a1a63", "openfda": {"unii": ["6871619Q5X"], "rxcui": ["314200"], "spl_set_id": ["a9b0d279-118b-4372-bd51-d4bad9c1cfca"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-051-20)  / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (51079-051-01)", "package_ndc": "51079-051-20", "marketing_start_date": "20110223"}], "brand_name": "Pantoprazole Sodium", "product_id": "51079-051_3a875ad3-8a73-b446-e063-6294a90a1a63", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "51079-051", "generic_name": "pantoprazole sodium", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pantoprazole Sodium", "active_ingredients": [{"name": "PANTOPRAZOLE SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA090970", "marketing_category": "ANDA", "marketing_start_date": "20110223", "listing_expiration_date": "20261231"}